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Previous release (v1)
2024-04-28 15:41:53, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_135290 569 bp RNA linear PRI 11-SEP-2020
DEFINITION Homo sapiens GCC2 antisense RNA 1 (GCC2-AS1), long non-coding RNA.
ACCESSION NR_135290
VERSION NR_135290.1
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 569)
AUTHORS Venter JC, Adams MD, Myers EW, Li PW, Mural RJ, Sutton GG, Smith
HO, Yandell M, Evans CA, Holt RA, Gocayne JD, Amanatides P, Ballew
RM, Huson DH, Wortman JR, Zhang Q, Kodira CD, Zheng XH, Chen L,
Skupski M, Subramanian G, Thomas PD, Zhang J, Gabor Miklos GL,
Nelson C, Broder S, Clark AG, Nadeau J, McKusick VA, Zinder N,
Levine AJ, Roberts RJ, Simon M, Slayman C, Hunkapiller M, Bolanos
R, Delcher A, Dew I, Fasulo D, Flanigan M, Florea L, Halpern A,
Hannenhalli S, Kravitz S, Levy S, Mobarry C, Reinert K, Remington
K, Abu-Threideh J, Beasley E, Biddick K, Bonazzi V, Brandon R,
Cargill M, Chandramouliswaran I, Charlab R, Chaturvedi K, Deng Z,
Di Francesco V, Dunn P, Eilbeck K, Evangelista C, Gabrielian AE,
Gan W, Ge W, Gong F, Gu Z, Guan P, Heiman TJ, Higgins ME, Ji RR, Ke
Z, Ketchum KA, Lai Z, Lei Y, Li Z, Li J, Liang Y, Lin X, Lu F,
Merkulov GV, Milshina N, Moore HM, Naik AK, Narayan VA, Neelam B,
Nusskern D, Rusch DB, Salzberg S, Shao W, Shue B, Sun J, Wang Z,
Wang A, Wang X, Wang J, Wei M, Wides R, Xiao C, Yan C, Yao A, Ye J,
Zhan M, Zhang W, Zhang H, Zhao Q, Zheng L, Zhong F, Zhong W, Zhu S,
Zhao S, Gilbert D, Baumhueter S, Spier G, Carter C, Cravchik A,
Woodage T, Ali F, An H, Awe A, Baldwin D, Baden H, Barnstead M,
Barrow I, Beeson K, Busam D, Carver A, Center A, Cheng ML, Curry L,
Danaher S, Davenport L, Desilets R, Dietz S, Dodson K, Doup L,
Ferriera S, Garg N, Gluecksmann A, Hart B, Haynes J, Haynes C,
Heiner C, Hladun S, Hostin D, Houck J, Howland T, Ibegwam C,
Johnson J, Kalush F, Kline L, Koduru S, Love A, Mann F, May D,
McCawley S, McIntosh T, McMullen I, Moy M, Moy L, Murphy B, Nelson
K, Pfannkoch C, Pratts E, Puri V, Qureshi H, Reardon M, Rodriguez
R, Rogers YH, Romblad D, Ruhfel B, Scott R, Sitter C, Smallwood M,
Stewart E, Strong R, Suh E, Thomas R, Tint NN, Tse S, Vech C, Wang
G, Wetter J, Williams S, Williams M, Windsor S, Winn-Deen E, Wolfe
K, Zaveri J, Zaveri K, Abril JF, Guigo R, Campbell MJ, Sjolander
KV, Karlak B, Kejariwal A, Mi H, Lazareva B, Hatton T, Narechania
A, Diemer K, Muruganujan A, Guo N, Sato S, Bafna V, Istrail S,
Lippert R, Schwartz R, Walenz B, Yooseph S, Allen D, Basu A,
Baxendale J, Blick L, Caminha M, Carnes-Stine J, Caulk P, Chiang
YH, Coyne M, Dahlke C, Mays A, Dombroski M, Donnelly M, Ely D,
Esparham S, Fosler C, Gire H, Glanowski S, Glasser K, Glodek A,
Gorokhov M, Graham K, Gropman B, Harris M, Heil J, Henderson S,
Hoover J, Jennings D, Jordan C, Jordan J, Kasha J, Kagan L, Kraft
C, Levitsky A, Lewis M, Liu X, Lopez J, Ma D, Majoros W, McDaniel
J, Murphy S, Newman M, Nguyen T, Nguyen N, Nodell M, Pan S, Peck J,
Peterson M, Rowe W, Sanders R, Scott J, Simpson M, Smith T, Sprague
A, Stockwell T, Turner R, Venter E, Wang M, Wen M, Wu D, Wu M, Xia
A, Zandieh A and Zhu X.
TITLE The sequence of the human genome
JOURNAL Science 291 (5507), 1304-1351 (2001)
PUBMED 11181995
REMARK Erratum:[Science 2001 Jun 5;292(5523):1838]
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AK095987.1 and BC004487.2.
##Evidence-Data-START##
Transcript exon combination :: BC004487.2, BX283893.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMN02400308 [ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-23 AK095987.1 1-23
24-569 BC004487.2 1-546
FEATURES Location/Qualifiers
source 1..569
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="2"
/map="2q12.3"
gene 1..569
/gene="GCC2-AS1"
/note="GCC2 antisense RNA 1"
/db_xref="GeneID:644903"
/db_xref="HGNC:HGNC:28126"
ncRNA 1..569
/ncRNA_class="lncRNA"
/gene="GCC2-AS1"
/product="GCC2 antisense RNA 1"
/db_xref="GeneID:644903"
/db_xref="HGNC:HGNC:28126"
exon 1..391
/gene="GCC2-AS1"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="GCC2-AS1"
/replace=""
/replace="a"
/db_xref="dbSNP:1684028014"
variation 1
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1558776201"
variation 2
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256459695"
variation 3
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684027720"
variation 6
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684027628"
variation 7
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2104554544"
variation 8
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1482880096"
variation 10..13
/gene="GCC2-AS1"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1684027313"
variation 12
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684027426"
variation 13
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1474717128"
variation 14
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684027111"
variation 16
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1255447003"
variation 19
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:966041871"
variation 21
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684026827"
variation 23
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1020189513"
variation 24
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684026524"
variation 25
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684026399"
variation 26
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:938886471"
variation 28
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:372511789"
variation 32
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2104554483"
variation 34
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010542058"
variation 35
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:928808620"
variation 36
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:980649934"
variation 40
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:893072362"
variation 42
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1684025450"
variation 43
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1033220468"
variation 44..52
/gene="GCC2-AS1"
/replace="gc"
/replace="gcgggtggc"
/db_xref="dbSNP:1684024531"
variation 45
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1684025212"
variation 46
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1310597968"
variation 47
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684025037"
variation 48
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1361842710"
variation 49
/gene="GCC2-AS1"
/replace=""
/replace="t"
/db_xref="dbSNP:1400260796"
variation 50
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:141912562"
variation 51
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1558776142"
variation 53
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1194952727"
variation 54..57
/gene="GCC2-AS1"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1684024269"
variation 54
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:970150635"
variation 58
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1573276755"
variation 59
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301718411"
variation 62
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339786034"
variation 65
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1230944087"
variation 66
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684023855"
variation 68
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1001377293"
variation 71
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489287142"
variation 72
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684023593"
variation 73
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217628598"
variation 74
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262673240"
variation 76
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1485007659"
variation 77
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:905603042"
variation 78
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1268469553"
variation 79
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:548187173"
variation 80
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776827921"
variation 81
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684022860"
variation 82
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1013909415"
variation 84
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2104554321"
variation 85..95
/gene="GCC2-AS1"
/replace="gcggcggcggc"
/replace="gcggcggcggcggc"
/db_xref="dbSNP:1438127170"
variation 85
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:879451155"
variation 86
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684022636"
variation 90
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1381634843"
variation 92
/gene="GCC2-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:2104554304"
variation 92
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1419716223"
variation 93
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157517120"
variation 95
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1443965371"
variation 97
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1293942131"
variation 98
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:896841292"
variation 99
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1036711277"
variation 101
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1573276599"
variation 102
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328620613"
variation 103
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684021871"
variation 105
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:956017182"
variation 110
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:940914645"
variation 111
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:909466135"
variation 112
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684021583"
variation 114..120
/gene="GCC2-AS1"
/replace="acaa"
/replace="acaacaa"
/db_xref="dbSNP:1223992462"
variation 115
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1241033639"
variation 118..148
/gene="GCC2-AS1"
/replace=""
/replace="caaggatggcggtgacgggcgcagggagcgg"
/db_xref="dbSNP:1684020173"
variation 118
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:6752142"
variation 121
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:932193322"
variation 122..132
/gene="GCC2-AS1"
/replace="ga"
/replace="gatggcggtga"
/db_xref="dbSNP:1684020890"
variation 122
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1008128930"
variation 128
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:922003219"
variation 129
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1684021029"
variation 131
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1383492536"
variation 132
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1684020822"
variation 133
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684020747"
variation 134
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:976168058"
variation 136
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:966168175"
variation 137
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369790911"
variation 138
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:566093605"
variation 143
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1164983869"
variation 146
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349090188"
variation 147
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1459624845"
variation 151
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684020098"
variation 153
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1333103144"
variation 154
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1684019951"
variation 155
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684019885"
variation 158
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1470641055"
variation 159
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1028169977"
variation 164
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232579174"
variation 166
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148115630"
variation 167
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1573276485"
variation 168
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684019178"
variation 170..175
/gene="GCC2-AS1"
/replace=""
/replace="aggctc"
/db_xref="dbSNP:1293643880"
variation 170
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684019114"
variation 173
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1230244889"
variation 175
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1481972682"
variation 178
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1334431308"
variation 183
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1684018628"
variation 185
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:56360832"
variation 187
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1358594107"
variation 191
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:957482494"
variation 192..194
/gene="GCC2-AS1"
/replace="g"
/replace="gtg"
/db_xref="dbSNP:1684018078"
variation 192
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224911248"
variation 193
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1558776024"
variation 198
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1198513478"
variation 200..217
/gene="GCC2-AS1"
/replace="gcggcc"
/replace="gcggccctggcagcggcc"
/db_xref="dbSNP:1684016855"
variation 200
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350751497"
variation 201
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:186344342"
variation 202
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684017667"
variation 204
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1182098013"
variation 205
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1001365791"
variation 210
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684017213"
variation 211
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1474018011"
variation 212
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1684017019"
variation 214
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1172605267"
variation 217
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684016782"
variation 218
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1573276367"
variation 219
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1684016656"
variation 221
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1347840276"
variation 222
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684016317"
variation 223..225
/gene="GCC2-AS1"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1684016146"
variation 223
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:550396769"
variation 225
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:531816950"
variation 226
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1304084313"
variation 227
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1404879088"
variation 229
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1355111631"
variation 230
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231665707"
variation 231
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1573276320"
variation 232
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280513242"
variation 235
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684015405"
variation 236
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2104553959"
variation 237
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1364185789"
variation 238
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:6723177"
variation 243..244
/gene="GCC2-AS1"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:1684015020"
variation 243
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1271426350"
variation 244
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684014937"
variation 247
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1573276290"
variation 250..272
/gene="GCC2-AS1"
/replace="cgcc"
/replace="cgccccgtcctggcgaggacgcc"
/db_xref="dbSNP:1684013518"
variation 250
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:886773161"
variation 253
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236349760"
variation 255
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684014507"
variation 256
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1013982770"
variation 257
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1048471215"
variation 258
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:896919845"
variation 262
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684014153"
variation 263
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1684014076"
variation 264
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684014007"
variation 266
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684013937"
variation 267
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1477340379"
variation 268
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1165931081"
variation 269
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1684013657"
variation 271
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037063454"
variation 276..280
/gene="GCC2-AS1"
/replace="ggggg"
/replace="gggggggg"
/db_xref="dbSNP:948832611"
variation 277
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:542929890"
variation 280
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1334993082"
variation 281
/gene="GCC2-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:2104553847"
variation 281
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:914694837"
variation 282
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341532180"
variation 283
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684012967"
variation 288
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684012883"
variation 290
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684012802"
variation 291
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:888026505"
variation 292
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684012652"
variation 293
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684012576"
variation 294
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1481513463"
variation 298
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1270819435"
variation 300
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347796596"
variation 301
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:529617111"
variation 302
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279034429"
variation 304
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:990232000"
variation 305
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:6709591"
variation 307
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:924621364"
variation 309
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:922076515"
variation 310
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1040540038"
variation 311
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1446065873"
variation 312
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1190816277"
variation 313
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684009902"
variation 317
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:987176410"
variation 322
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478329981"
variation 324
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684009658"
variation 325
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684009596"
variation 326
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684009533"
variation 328
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684009464"
variation 329
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:540711113"
variation 330
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:955336035"
variation 331
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684009268"
variation 332
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1028618776"
variation 333
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1432876392"
variation 337
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:944750261"
variation 338
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:114609913"
variation 339
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684008875"
variation 341
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684008808"
variation 344
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381832777"
variation 345
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1684008676"
variation 346
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1684008618"
variation 348
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:989211463"
variation 350
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:558467307"
variation 351
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1684008369"
variation 353
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:540279713"
variation 354
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303242936"
variation 355
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016677436"
variation 356..370
/gene="GCC2-AS1"
/replace="g"
/replace="gagctccgcatggag"
/db_xref="dbSNP:1684007556"
variation 358
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1369413156"
variation 359
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1284336398"
variation 360
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780683144"
variation 361
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:543555239"
variation 365
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1684007698"
variation 366
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684007631"
variation 370
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1684007484"
variation 371
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1349571307"
variation 372
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:200289564"
variation 373
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432079605"
variation 377
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:980043602"
variation 378
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1684006542"
variation 379
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251123148"
variation 380..386
/gene="GCC2-AS1"
/replace="ttt"
/replace="tttgttt"
/db_xref="dbSNP:748552112"
variation 381..387
/gene="GCC2-AS1"
/replace=""
/replace="ttgttta"
/db_xref="dbSNP:1316262689"
variation 381
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1684006386"
variation 384
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:969975413"
variation 386
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1684006180"
variation 390
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1453347117"
variation 391
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156978646"
exon 392..474
/gene="GCC2-AS1"
/inference="alignment:Splign:2.1.0"
variation 393
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1683464261"
variation 394..400
/gene="GCC2-AS1"
/replace="aaa"
/replace="aaagaaa"
/db_xref="dbSNP:1194908860"
variation 395
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:528842058"
variation 400
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1377953063"
variation 403
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1037426547"
variation 404
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366843525"
variation 405
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1300620805"
variation 406
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:941772538"
variation 410
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:182329924"
variation 411
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:930275837"
variation 414
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:542927243"
variation 419..426
/gene="GCC2-AS1"
/replace="aagaa"
/replace="aagaagaa"
/db_xref="dbSNP:199901241"
variation 419
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1683463306"
variation 420
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461850104"
variation 421..422
/gene="GCC2-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:1683462667"
variation 421
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1183015078"
variation 424
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1573258633"
variation 425
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1241549314"
variation 430
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1683462379"
variation 432
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1683462320"
variation 433
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238970703"
variation 434
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352078002"
variation 437
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1683462077"
variation 439
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1683462017"
variation 440
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:982346429"
variation 443
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370294833"
variation 444
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:969561461"
variation 445
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1683461669"
variation 450
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384121123"
variation 454
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386951702"
variation 455
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:528128657"
variation 460
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1683459809"
variation 467
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1023777748"
variation 469
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:3098321"
variation 472
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1358503516"
variation 473
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1235089839"
variation 474
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1683459581"
exon 475..569
/gene="GCC2-AS1"
/inference="alignment:Splign:2.1.0"
variation 476..477
/gene="GCC2-AS1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1683267486"
variation 476
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1683267625"
variation 477
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044948041"
variation 479
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1221123431"
variation 481
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1683267061"
variation 482
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1330074691"
variation 485
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1323794297"
variation 487
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760913258"
variation 488
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1393885010"
variation 490
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329679925"
variation 491
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:773530396"
variation 494
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424940430"
variation 496
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1683265378"
variation 497
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:772397145"
variation 502
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477078252"
variation 505
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1429175725"
variation 514
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1683264485"
variation 515
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:148220751"
variation 516
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448580295"
variation 517
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200257241"
variation 518
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449274621"
variation 520
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1283995110"
variation 524
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253258219"
variation 527
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1683262911"
variation 528
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:769206694"
variation 530
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:745310946"
variation 532
/gene="GCC2-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2104526956"
variation 533
/gene="GCC2-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1683262550"
variation 535
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:780774991"
variation 536
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:572432590"
variation 537
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1683262179"
variation 540
/gene="GCC2-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1197760492"
variation 541
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1458081723"
variation 542
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1259912674"
variation 543..545
/gene="GCC2-AS1"
/replace="aaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaaa"
/db_xref="dbSNP:rs1573251903"
variation 543
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1683261817"
variation 546..547
/gene="GCC2-AS1"
/replace=""
/replace="gt"
/db_xref="dbSNP:781695108"
variation 546
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756928902"
variation 547
/gene="GCC2-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:746628485"
variation 548..551
/gene="GCC2-AS1"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:754450461"
variation 549..555
/gene="GCC2-AS1"
/replace="aaacaaa"
/replace="aaacaaacaaa"
/db_xref="dbSNP:1553445748"
variation 550..554
/gene="GCC2-AS1"
/replace="aacaa"
/replace="aacaacaa"
/db_xref="dbSNP:1553445755"
variation 552
/gene="GCC2-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:1573251855"
variation 552
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:201181021"
variation 552
/gene="GCC2-AS1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:751139050"
variation 553..563
/gene="GCC2-AS1"
/replace="aaaaaaa"
/replace="aaaaaaaaa"
/replace="aaaaaaaaaa"
/replace="aaaaaaaaaaa"
/replace="aaaaaaaaaaaa"
/replace="aaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaa"
/db_xref="dbSNP:rs201688853"
variation 553..563
/gene="GCC2-AS1"
/replace=""
/replace="aaaaaaaaaaa"
/db_xref="dbSNP:1235530697"
variation 553
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:777616862"
variation 554..555
/gene="GCC2-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:567535770"
variation 554
/gene="GCC2-AS1"
/replace="a"
/replace="aca"
/db_xref="dbSNP:1553445754"
variation 554
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:867123486"
variation 555..556
/gene="GCC2-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:761559026"
variation 555
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:758255170"
variation 556
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2577596"
variation 558
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1683259188"
variation 560..561
/gene="GCC2-AS1"
/replace=""
/replace="g"
/db_xref="dbSNP:753727652"
variation 560
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274856114"
variation 562..563
/gene="GCC2-AS1"
/replace=""
/replace="c"
/db_xref="dbSNP:528390908"
variation 564..565
/gene="GCC2-AS1"
/replace=""
/replace="t"
/db_xref="dbSNP:1683257871"
variation 564
/gene="GCC2-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:112578582"
variation 566
/gene="GCC2-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1573251676"
ORIGIN
atttcagcaccccaggctagtctgggaggctggcgcaaacgcagcgggtggctggggtaggggctcattgggagcccacggagcgcggcggcggctcgggggccgagttccctacaacaaggatggcggtgacgggcgcagggagcggggcccggctctccttgcctcgaggctcctctgattccactcgcgtggctgcgcggccctggcagcggccttcgtcccgggggtgggagctacacagggttccgccccgtcctggcgaggacgcctgagggggctctgtggtaaggctctgtcgggcaggccgggcttccgggaggacctggtctggatcggtcaccgctgggtgcctgagctccgcatggagcctgcagcctttgtttaacttataaagaaatgggggctccgagcagtcaagaagaacatgccccaagttattcgtcagtgaggcggaaattgtggtgtacttgttccagaccaactatgaagataggatgcccatccagaagaacgggaagcattttcttcctcacctttggaaagtaaaacaaaaaaaaaaagaaaaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]