2024-03-29 17:18:54, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_146574 529 bp RNA linear PRI 19-APR-2022 DEFINITION Homo sapiens long intergenic non-protein coding RNA 2136 (LINC02136), long non-coding RNA. ACCESSION NR_146574 XR_001733696 XR_001752335 VERSION NR_146574.1 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 529) AUTHORS Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R, Yamamoto J, Sekine M, Tsuritani K, Wakaguri H, Ishii S, Sugiyama T, Saito K, Isono Y, Irie R, Kushida N, Yoneyama T, Otsuka R, Kanda K, Yokoi T, Kondo H, Wagatsuma M, Murakawa K, Ishida S, Ishibashi T, Takahashi-Fujii A, Tanase T, Nagai K, Kikuchi H, Nakai K, Isogai T and Sugano S. TITLE Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes JOURNAL Genome Res. 16 (1), 55-65 (2006) PUBMED 16344560 COMMENT PREDICTED REFSEQ: This record has not been reviewed and the function is unknown. The reference sequence was derived from DA211558.1. On or before Apr 8, 2017 this sequence version replaced XR_001752335.1, XR_001733696.1. ##Evidence-Data-START## Transcript exon combination :: DA211558.1, SRR5189667.328160.1 [ECO:0000332] RNAseq introns :: mixed sample support SAMEA1968968, SAMEA2148093 [ECO:0006172] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-529 DA211558.1 1-529 FEATURES Location/Qualifiers source 1..529 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="16" /map="16q22.2" gene 1..529 /gene="LINC02136" /note="long intergenic non-protein coding RNA 2136" /db_xref="GeneID:105371333" /db_xref="HGNC:HGNC:52995" ncRNA 1..529 /ncRNA_class="lncRNA" /gene="LINC02136" /product="long intergenic non-protein coding RNA 2136" /db_xref="GeneID:105371333" /db_xref="HGNC:HGNC:52995" exon 1..304 /gene="LINC02136" /inference="alignment:Splign:2.1.0" variation 1 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:527917128" variation 3 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:909497721" variation 5 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:1348837210" variation 8 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042779908" variation 10 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1438058883" variation 11 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042779889" variation 12 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1596981591" variation 13 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1327512596" variation 17 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042779868" variation 18 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2042779858" variation 19 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2042779849" variation 20 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1371188546" variation 21 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:1382037928" variation 22 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:566741310" variation 24 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1454734692" variation 25 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:11644434" variation 26 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1156711975" variation 28 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2042779793" variation 30 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2145038678" variation 31 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1268738559" variation 32 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1009940050" variation 33 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2042779765" variation 34 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042779755" variation 35 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:956642104" variation 36 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2042779659" variation 37 /gene="LINC02136" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1289785081" variation 38 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:927725374" variation 39 /gene="LINC02136" /replace="a" /replace="aa" /db_xref="dbSNP:2042779630" variation 39 /gene="LINC02136" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:530216187" variation 40 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:879450429" variation 41 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2042779598" variation 42 /gene="LINC02136" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1215575730" variation 43 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1253873871" variation 44 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:74499657" variation 45 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1192238854" variation 46 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:971945785" variation 48 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1023144075" variation 49 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:753503837" variation 52 /gene="LINC02136" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:562700647" variation 56 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:904512060" variation 58 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1459415536" variation 59 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:1166412609" variation 61 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1442247446" variation 63 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:957683148" variation 65 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1315749757" variation 67 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1431913203" variation 68 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:763778908" variation 70 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042779339" variation 71 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:996905086" variation 73 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:2042779325" variation 76 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2145038625" variation 83..86 /gene="LINC02136" /replace="ccc" /replace="cccc" /db_xref="dbSNP:2042779288" variation 83 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1032968001" variation 84 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:901337674" variation 85 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1241945271" variation 86 /gene="LINC02136" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:143579975" variation 88 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1203656624" variation 89 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1462416040" variation 90 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1596981496" variation 92 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:746298997" variation 95 /gene="LINC02136" /replace="g" /replace="gg" /db_xref="dbSNP:1193547699" variation 96 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:1029677256" variation 97 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:531503565" variation 98 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2042779202" variation 99 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1215593019" variation 102 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2042779190" variation 103 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:1256751090" variation 106 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:1474154762" variation 107 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042779173" variation 108 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1447882405" variation 109 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:1596981481" variation 110 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2145038589" variation 112 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2042779152" variation 113 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1417999326" variation 121 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042779135" variation 122 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:2145038573" variation 123 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:2042779130" variation 125 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2042779123" variation 127 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:998294111" variation 131 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2042779105" variation 132 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042779095" variation 133 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2042779083" variation 142 /gene="LINC02136" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2042779075" variation 143 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:9930764" variation 144 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1039540038" variation 151 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1358841835" variation 154 /gene="LINC02136" /replace="" /replace="a" /db_xref="dbSNP:2042779027" variation 154 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:941270839" variation 156 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1354139426" variation 157 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:533982315" variation 163 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1048113222" variation 164..167 /gene="LINC02136" /replace="ccc" /replace="cccc" /replace="cccccc" /db_xref="dbSNP:1262716149" variation 165 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:888397301" variation 166 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2042778967" variation 167 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1236961317" variation 168 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:546003698" variation 170 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2042778936" variation 171 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2042778929" variation 172 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:926248083" variation 173 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:771103910" variation 174 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042778896" variation 175 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042778883" variation 176 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:980519664" variation 177 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:970501657" variation 179 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1213019551" variation 182 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2042778847" variation 185 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:2042778837" variation 186 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1046750062" variation 188 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:929607100" variation 191 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1178967566" variation 192 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1429791493" variation 194 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1470281291" variation 195 /gene="LINC02136" /replace="a" /replace="t" /db_xref="dbSNP:1172603330" variation 196 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:1345500445" variation 197 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:138032761" variation 198 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042778773" variation 199 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2042778765" variation 202 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1422616177" variation 204 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:981826186" variation 205 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1596981407" variation 206 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:150313829" variation 209..223 /gene="LINC02136" /replace="gggacccgggacccg" /replace="gggacccgggacccgggacccg" /db_xref="dbSNP:1163710831" variation 211 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1389773826" variation 214 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1567554396" variation 215 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2042778700" variation 216 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:916062289" variation 217 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1032240746" variation 218 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042778674" variation 223 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:991705748" variation 224 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1301518581" variation 225 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1345537620" variation 227 /gene="LINC02136" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:957844455" variation 228 /gene="LINC02136" /replace="a" /replace="t" /db_xref="dbSNP:1212680837" variation 230 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1033248594" variation 231 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042778596" variation 233 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:2042778591" variation 234 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042778585" variation 236 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:2042778581" variation 242 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:968696415" variation 243 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2042778562" variation 244 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1280963681" variation 245 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042778538" variation 248 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:374115085" variation 249 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:1028238484" variation 252 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:2042778507" variation 253 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:977661678" variation 254 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:997377506" variation 257 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1192698374" variation 259 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:2042778430" variation 264 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042778423" variation 266 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:967321408" variation 267 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:2042778412" variation 268 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:901248737" variation 269 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:1041637545" variation 270 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042778382" variation 274 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1185506196" variation 275 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:1174609983" variation 277 /gene="LINC02136" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1004365424" variation 278 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2145038459" variation 283..284 /gene="LINC02136" /replace="g" /replace="gg" /db_xref="dbSNP:779747787" variation 283 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1460958716" variation 286 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1029626368" variation 290 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1324151505" variation 292 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:998638485" variation 292 /gene="LINC02136" /replace="t" /replace="tt" /db_xref="dbSNP:2042778308" variation 294 /gene="LINC02136" /replace="a" /replace="t" /db_xref="dbSNP:1680417125" variation 299 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1048690072" variation 302 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:931514578" exon 305..435 /gene="LINC02136" /inference="alignment:Splign:2.1.0" variation 305 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:981202412" variation 308 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:993410704" variation 309 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:1596976730" variation 317 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1162042259" variation 320 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1368060535" variation 328 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042738764" variation 329 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1596976723" variation 330 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1406053334" variation 333 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2042738722" variation 334 /gene="LINC02136" /replace="a" /replace="t" /db_xref="dbSNP:1288753175" variation 336 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042738698" variation 338 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:946754232" variation 339 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:915280407" variation 340 /gene="LINC02136" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:143936282" variation 344 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1382296057" variation 345 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:988254006" variation 355 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1289290297" variation 360 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042738598" variation 362 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1027972871" variation 363 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2145032050" variation 364..366 /gene="LINC02136" /replace="aa" /replace="aaa" /db_xref="dbSNP:996501656" variation 365 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1222251305" variation 367 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1484610940" variation 368 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:900930672" variation 369 /gene="LINC02136" /replace="" /replace="c" /db_xref="dbSNP:1040764910" variation 369 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2042738490" variation 372 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:1443602767" variation 381..383 /gene="LINC02136" /replace="gg" /replace="ggg" /db_xref="dbSNP:1188979198" variation 382 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1256858321" variation 384..387 /gene="LINC02136" /replace="aaa" /replace="aaaa" /db_xref="dbSNP:939851542" variation 391 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1280550304" variation 394 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:543534422" variation 405 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1567552334" variation 413 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1343877634" variation 414 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:956489526" variation 418 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1455466892" variation 420 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1289502750" variation 424 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2145032026" variation 428 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:2042738322" variation 433 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1382360996" variation 434 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1450770749" exon 436..529 /gene="LINC02136" /inference="alignment:Splign:2.1.0" variation 436 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:933026342" variation 438 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2042721646" variation 441 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:545505819" variation 446 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:2042721627" variation 447 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:2145029246" variation 460 /gene="LINC02136" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2042721617" variation 461 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1596974791" variation 462 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:2042721593" variation 466 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1402114369" variation 467 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:1226190976" variation 468 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:2042721568" variation 471 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042721557" variation 473 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:2042721553" variation 474..491 /gene="LINC02136" /replace="cag" /replace="caggaaggggcctggcag" /db_xref="dbSNP:1234739984" variation 477 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:577911287" variation 479 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042721540" variation 483 /gene="LINC02136" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1302568957" variation 484 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:1328899742" variation 488 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042721522" variation 490 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:2042721513" variation 491 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:1596974773" variation 494..495 /gene="LINC02136" /replace="" /replace="tg" /db_xref="dbSNP:2042721490" variation 496 /gene="LINC02136" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:937789649" variation 504 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042721467" variation 505 /gene="LINC02136" /replace="g" /replace="t" /db_xref="dbSNP:971815473" variation 506 /gene="LINC02136" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1196305959" variation 508 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:760729622" variation 510 /gene="LINC02136" /replace="a" /replace="c" /db_xref="dbSNP:2145029203" variation 512 /gene="LINC02136" /replace="a" /replace="t" /db_xref="dbSNP:775534297" variation 517 /gene="LINC02136" /replace="c" /replace="g" /db_xref="dbSNP:1458492716" variation 518 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042721398" variation 522 /gene="LINC02136" /replace="a" /replace="g" /db_xref="dbSNP:2042721390" variation 523 /gene="LINC02136" /replace="" /replace="c" /db_xref="dbSNP:1213689792" variation 526..529 /gene="LINC02136" /replace="a" /replace="atta" /db_xref="dbSNP:2042721361" variation 527 /gene="LINC02136" /replace="c" /replace="t" /db_xref="dbSNP:1251659935" ORIGIN
gtaagaaaatgcctgcagccccttgcactcgcggagtcatctacgcaaggtcgggctctgcaggcagcagcttctggtctcaccccgggcttgtgcgcacacctggggacatgtgggaaggtcgctcttgcggccactgagcggcctggcctcagggaacgagccccgcgccgggaagaaagctgcctgccgggagcgcagcctattggggacccgggacccgagccaccgcggctcaccaagaggcggtggggccctgcggtgcgtgtgggacgccgggcaggcagactctgagcacggccaggaggcaagaagagattgaagggaaatctcaaggggctccagagactactacgatggtgcaaagtcacagaagccctgggaaaagcaggtagaatggagttgccatgacattgagcctcacctagatgccagttccagatattggcagactgctggcctcctgaggagcacaggaaggggcctggcagactggtgatcctggttggagatgaagaggggctgatta
//
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.
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