Linked Data
ClinVar Variation Id:
1914333
ClinVar RCV Id:
RCV002597469
dbSNP Id:
rs146156900
ExAC:
9:4118662 G / A
gnomAD v2:
9-4118662-G-A
gnomAD v3:
9-4118662-G-A
gnomAD v4:
9-4118662-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.4118662G>A , CM000671.2:g.4118662G>A | GRCh38 |
| NC_000009.11:g.4118662G>A , CM000671.1:g.4118662G>A | GRCh37 |
| NC_000009.10:g.4108662G>A | NCBI36 |
| NG_011782.1:g.186374C>T | |
| NG_011782.2:g.186374C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000491889.6:c.*179C>T | ENSP00000419914.1:n.*179C>T | |
| ENST00000645252.2:n.152+32278C>T | ||
| ENST00000682749.1:c.351C>T | ENSP00000507306.1:p.Tyr117= | |
| ENST00000682846.1:c.131+7072C>T | ENSP00000507527.1:n.131+7072C>T | |
| ENST00000381971.8:c.816C>T MANE Select | ENSP00000371398.3:p.Tyr272= | |
| ENST00000645252.1:n.152+32278C>T | ||
| ENST00000324333.14:c.351C>T | ENSP00000325494.10:p.Tyr117= | |
| ENST00000381971.7:c.816C>T | ENSP00000371398.3:p.Tyr272= | |
| ENST00000490709.1:n.636C>T | ||
| NM_001042413.1:c.816C>T | NP_001035878.1:p.Tyr272= | |
| NM_152629.3:c.351C>T | NP_689842.3:p.Tyr117= | |
| XM_005251386.3:c.351C>T | XP_005251443.1:p.Tyr117= | |
| XM_005251387.3:c.150C>T | XP_005251444.1:p.Tyr50= | |
| XM_005251388.3:c.150C>T | XP_005251445.1:p.Tyr50= | |
| XM_005251389.3:c.816C>T | XP_005251446.1:p.Tyr272= | |
| XM_006716731.2:c.816C>T | XP_006716794.1:p.Tyr272= | |
| XM_011517763.1:c.816C>T | XP_011516065.1:p.Tyr272= | |
| XM_011517764.1:c.816C>T | XP_011516066.1:p.Tyr272= | |
| XM_011517765.1:c.816C>T | XP_011516067.1:p.Tyr272= | |
| XM_011517766.1:c.351C>T | XP_011516068.1:p.Tyr117= | |
| XM_011517767.1:c.150C>T | XP_011516069.1:p.Tyr50= | |
| XM_011517768.1:c.816C>T | XP_011516070.1:p.Tyr272= | |
| XM_011517769.1:c.816C>T | XP_011516071.1:p.Tyr272= | |
| XR_929206.1:n.1582C>T | ||
| XM_005251386.4:c.351C>T | XP_005251443.1:p.Tyr117= | |
| XM_005251387.4:c.150C>T | XP_005251444.1:p.Tyr50= | |
| XM_005251388.4:c.150C>T | XP_005251445.1:p.Tyr50= | |
| XM_005251389.5:c.816C>T | XP_005251446.1:p.Tyr272= | |
| XM_006716731.3:c.816C>T | XP_006716794.1:p.Tyr272= | |
| XM_011517763.2:c.816C>T | XP_011516065.1:p.Tyr272= | |
| XM_011517764.2:c.816C>T | XP_011516066.1:p.Tyr272= | |
| XM_011517765.2:c.816C>T | XP_011516067.1:p.Tyr272= | |
| XM_011517766.2:c.351C>T | XP_011516068.1:p.Tyr117= | |
| XM_011517767.3:c.150C>T | XP_011516069.1:p.Tyr50= | |
| XM_011517769.2:c.816C>T | XP_011516071.1:p.Tyr272= | |
| XM_017014361.1:c.351C>T | XP_016869850.1:p.Tyr117= | |
| XR_929206.2:n.1578C>T | ||
| NM_001042413.2:c.816C>T MANE Select | NP_001035878.1:p.Tyr272= | |
| NM_152629.4:c.351C>T | NP_689842.3:p.Tyr117= |