Linked Data
ClinVar Variation Id:
515851
dbSNP Id:
rs542523863
ExAC:
15:42698153 G / A
gnomAD v2:
15-42698153-G-A
gnomAD v3:
15-42405955-G-A
gnomAD v4:
15-42405955-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42405955G>A , CM000677.2:g.42405955G>A | GRCh38 |
| NC_000015.9:g.42698153G>A , CM000677.1:g.42698153G>A | GRCh37 |
| NC_000015.8:g.40485445G>A | NCBI36 |
| NG_008660.1:g.62853G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337571.9:c.-82+987G>A | ENSP00000336840.4:n.-82+987G>A | |
| ENST00000349748.8:c.1638+2178G>A | ENSP00000183936.4:n.1638+2178G>A | |
| ENST00000357568.8:c.1782+2178G>A | ENSP00000350181.3:n.1782+2178G>A | |
| ENST00000397163.8:c.1800+12G>A MANE Select | ENSP00000380349.3:n.1800+12G>A | |
| ENST00000397204.9:c.-82+12G>A | ENSP00000380387.4:n.-82+12G>A | |
| ENST00000466369.5:n.2291+2178G>A | ||
| ENST00000495723.1:n.2671+2178G>A | ||
| ENST00000549793.5:n.2013+2178G>A | ||
| ENST00000565173.2:n.174+1000G>A | ||
| ENST00000569136.6:c.-196+12G>A | ENSP00000455254.1:n.-196+12G>A | |
| ENST00000638141.2:n.1653+2178G>A | ||
| ENST00000673646.1:c.364+12G>A | ENSP00000501007.1:n.364+12G>A | |
| ENST00000673692.1:c.-4+1104G>A | ENSP00000501138.1:n.-4+1104G>A | |
| ENST00000673705.1:c.310-3348G>A | ENSP00000501021.1:n.310-3348G>A | |
| ENST00000673743.1:c.-437+1000G>A | ENSP00000500989.1:n.-437+1000G>A | |
| ENST00000673750.1:c.-2451G>A | ENSP00000501173.1:n.-2451G>A | |
| ENST00000673771.1:c.-196+987G>A | ENSP00000501023.1:n.-196+987G>A | |
| ENST00000673839.1:c.-340+1000G>A | ENSP00000501188.1:n.-340+1000G>A | |
| ENST00000673851.1:c.-540+12G>A | ENSP00000501142.1:n.-540+12G>A | |
| ENST00000673854.1:n.1989G>A | ||
| ENST00000673886.1:c.-928-742G>A | ENSP00000501155.1:n.-928-742G>A | |
| ENST00000673890.1:c.-196+1000G>A | ENSP00000501293.1:n.-196+1000G>A | |
| ENST00000673928.1:c.-340+1000G>A | ENSP00000501099.1:n.-340+1000G>A | |
| ENST00000673936.1:c.-196+1104G>A | ENSP00000501189.1:n.-196+1104G>A | |
| ENST00000673939.1:c.-82+1000G>A | ENSP00000501129.1:n.-82+1000G>A | |
| ENST00000673978.1:c.-362+1000G>A | ENSP00000500976.1:n.-362+1000G>A | |
| ENST00000673987.1:c.-196+12G>A | ENSP00000501231.1:n.-196+12G>A | |
| ENST00000674011.1:c.-196+1000G>A | ENSP00000501171.1:n.-196+1000G>A | |
| ENST00000674012.1:n.75+987G>A | ||
| ENST00000674018.1:c.-540+987G>A | ENSP00000501271.1:n.-540+987G>A | |
| ENST00000674041.1:c.-82+1000G>A | ENSP00000500956.1:n.-82+1000G>A | |
| ENST00000674052.1:c.24+12G>A | ENSP00000501057.1:n.24+12G>A | |
| ENST00000674064.1:n.179+1000G>A | ||
| ENST00000674093.1:c.-82+1000G>A | ENSP00000501303.1:n.-82+1000G>A | |
| ENST00000674119.1:c.-82+1104G>A | ENSP00000501217.1:n.-82+1104G>A | |
| ENST00000674135.1:c.-132+1000G>A | ENSP00000501178.1:n.-132+1000G>A | |
| ENST00000674139.1:c.-2451G>A | ENSP00000501054.1:n.-2451G>A | |
| ENST00000674146.1:c.-524+12G>A | ENSP00000501175.1:n.-524+12G>A | |
| ENST00000674149.1:c.-524+1000G>A | ENSP00000501112.1:n.-524+1000G>A | |
| ENST00000318023.11:c.1656+12G>A | ENSP00000326281.8:n.1656+12G>A | |
| ENST00000337571.8:c.-82+1000G>A | ENSP00000336840.4:n.-82+1000G>A | |
| ENST00000349748.7:c.1638+2178G>A | ENSP00000183936.4:n.1638+2178G>A | |
| ENST00000356316.7:c.-91+991G>A | ENSP00000348667.4:n.-91+991G>A | |
| ENST00000357568.7:c.1782+2178G>A | ENSP00000350181.3:n.1782+2178G>A | |
| ENST00000397163.7:c.1800+12G>A | ENSP00000380349.3:n.1800+12G>A | |
| ENST00000397200.8:c.264+12G>A | ENSP00000380384.4:n.264+12G>A | |
| ENST00000397204.8:c.-82+12G>A | ENSP00000380387.4:n.-82+12G>A | |
| ENST00000561817.5:c.-82+1000G>A | ENSP00000456575.1:n.-82+1000G>A | |
| ENST00000565173.1:n.129+1000G>A | ||
| ENST00000565274.5:c.12+12G>A | ENSP00000457759.1:n.12+12G>A | |
| ENST00000565559.5:c.-132+12G>A | ENSP00000457878.1:n.-132+12G>A | |
| ENST00000567071.5:c.259+12G>A | ||
| ENST00000569136.5:c.-196+12G>A | ENSP00000455254.1:n.-196+12G>A | |
| ENST00000569827.5:c.246+2178G>A | ENSP00000454379.1:n.246+2178G>A | |
| NM_000070.2:c.1800+12G>A | NP_000061.1:n.1800+12G>A | |
| NM_024344.1:c.1782+2178G>A | NP_077320.1:n.1782+2178G>A | |
| NM_173087.1:c.1638+2178G>A | NP_775110.1:n.1638+2178G>A | |
| NM_173088.1:c.264+12G>A | NP_775111.1:n.264+12G>A | |
| NM_173089.1:c.-82+1000G>A | NP_775112.1:n.-82+1000G>A | |
| NM_173090.1:c.-82+12G>A | NP_775113.1:n.-82+12G>A | |
| NM_000070.3:c.1800+12G>A MANE Select | NP_000061.1:n.1800+12G>A | |
| NM_024344.2:c.1782+2178G>A | NP_077320.1:n.1782+2178G>A | |
| NM_173087.2:c.1638+2178G>A | NP_775110.1:n.1638+2178G>A | |
| NM_173088.2:c.264+12G>A | NP_775111.1:n.264+12G>A | |
| NM_173089.2:c.-82+1000G>A | NP_775112.1:n.-82+1000G>A | |
| NM_173090.2:c.-82+12G>A | NP_775113.1:n.-82+12G>A |