Linked Data
ClinVar Variation Id:
228354
ClinVar RCV Id:
RCV000218080
dbSNP Id:
rs773068151
ExAC:
1:109446746 G / T
gnomAD v2:
1-109446746-G-T
gnomAD v3:
1-108904124-G-T
gnomAD v4:
1-108904124-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.108904124G>T , CM000663.2:g.108904124G>T | GRCh38 |
| NC_000001.10:g.109446746G>T , CM000663.1:g.109446746G>T | GRCh37 |
| NC_000001.9:g.109248269G>T | NCBI36 |
| NG_028108.1:g.32144G>T | |
| NG_028108.2:g.33775G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000690509.1:c.*46-21876C>A (CLCC1) | ENSP00000510142.1:n.*46-21876C>A | |
| ENST00000264126.9:c.1063-1G>T (GPSM2) MANE Select | ENSP00000264126.3:n.1063-1G>T | |
| ENST00000357393.6:c.1-54548C>A (AKNAD1) | ENSP00000349968.6:n.1-54548C>A | |
| ENST00000441735.2:c.1063-1G>T (GPSM2) | ENSP00000390629.2:n.1063-1G>T | |
| ENST00000446797.2:c.1063-1G>T (GPSM2) | ENSP00000392138.2:n.1063-1G>T | |
| ENST00000642355.1:c.1063-1G>T (GPSM2) | ENSP00000496104.1:n.1063-1G>T | |
| ENST00000643643.1:c.152-1G>T (GPSM2) | ||
| ENST00000643921.1:n.66-1G>T (GPSM2) | ||
| ENST00000645164.2:c.1063-1G>T (GPSM2) | ENSP00000496756.2:n.1063-1G>T | |
| ENST00000645255.1:c.585-1G>T (GPSM2) | ||
| ENST00000674700.1:c.1006-1G>T (GPSM2) | ENSP00000501743.1:n.1006-1G>T | |
| ENST00000674731.1:c.1006-1G>T (GPSM2) | ENSP00000502401.1:n.1006-1G>T | |
| ENST00000674914.1:c.1114-1G>T (GPSM2) | ENSP00000501579.1:n.1114-1G>T | |
| ENST00000675086.1:c.1063-1G>T (GPSM2) | ENSP00000502476.1:n.1063-1G>T | |
| ENST00000675087.1:c.1114-1G>T (GPSM2) | ENSP00000502020.1:n.1114-1G>T | |
| ENST00000675617.1:n.1625-1G>T (GPSM2) | ||
| ENST00000675740.1:n.837G>T (GPSM2) | ||
| ENST00000675776.1:n.2447G>T (GPSM2) | ||
| ENST00000676184.1:c.1063-1G>T (GPSM2) | ENSP00000502178.1:n.1063-1G>T | |
| ENST00000676404.1:c.1006-1G>T (GPSM2) | ENSP00000502346.1:n.1006-1G>T | |
| ENST00000264126.7:c.1063-1G>T (GPSM2) | ENSP00000264126.3:n.1063-1G>T | |
| ENST00000357393.5:c.115-54548C>A | ENSP00000349968.5:n.115-54548C>A | |
| ENST00000406462.6:c.1063-1G>T (GPSM2) | ENSP00000385510.1:n.1063-1G>T | |
| NM_013296.4:c.1063-1G>T (GPSM2) | NP_037428.3:n.1063-1G>T | |
| XM_005270787.2:c.1063-1G>T (GPSM2) | XP_005270844.1:n.1063-1G>T | |
| XM_006710589.1:c.1006-1G>T (GPSM2) | XP_006710652.1:n.1006-1G>T | |
| XM_011541301.1:c.1063-1G>T (GPSM2) | XP_011539603.1:n.1063-1G>T | |
| XM_011541302.1:c.1063-1G>T (GPSM2) | XP_011539604.1:n.1063-1G>T | |
| XM_011541303.1:c.1063-1G>T (GPSM2) | XP_011539605.1:n.1063-1G>T | |
| NM_001321038.1:c.1063-1G>T (GPSM2) | NP_001307967.1:n.1063-1G>T | |
| NM_001321039.1:c.1063-1G>T (GPSM2) | NP_001307968.1:n.1063-1G>T | |
| XM_006710589.3:c.1006-1G>T (GPSM2) | XP_006710652.1:n.1006-1G>T | |
| XM_011541301.2:c.1063-1G>T (GPSM2) | XP_011539603.1:n.1063-1G>T | |
| XM_011541302.3:c.1063-1G>T (GPSM2) | XP_011539604.1:n.1063-1G>T | |
| XM_011541303.3:c.1063-1G>T (GPSM2) | XP_011539605.1:n.1063-1G>T | |
| XM_017001097.2:c.1063-1G>T (GPSM2) | XP_016856586.1:n.1063-1G>T | |
| XM_017001098.2:c.1063-1G>T (GPSM2) | XP_016856587.1:n.1063-1G>T | |
| NM_013296.5:c.1063-1G>T (GPSM2) MANE Select | NP_037428.3:n.1063-1G>T | |
| NM_001321038.2:c.1063-1G>T (GPSM2) | NP_001307967.1:n.1063-1G>T | |
| NM_001321039.2:c.1063-1G>T (GPSM2) | NP_001307968.1:n.1063-1G>T | |
| NM_001321039.3:c.1063-1G>T (GPSM2) | NP_001307968.1:n.1063-1G>T |