Linked Data
ClinVar Variation Id:
711683
ClinVar RCV Id:
RCV000883484
dbSNP Id:
rs6662340
ExAC:
1:7724413 G / A
gnomAD v2:
1-7724413-G-A
gnomAD v3:
1-7664353-G-A
gnomAD v4:
1-7664353-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.7664353G>A , CM000663.2:g.7664353G>A | GRCh38 |
| NC_000001.10:g.7724413G>A , CM000663.1:g.7724413G>A | GRCh37 |
| NC_000001.9:g.7647000G>A | NCBI36 |
| NG_053148.1:g.884030G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476864.2:c.1806G>A | ENSP00000452319.2:p.Thr602= | |
| ENST00000700414.1:c.*1657G>A | ENSP00000514978.1:n.*1657G>A | |
| ENST00000700415.1:c.1716G>A | ENSP00000514979.1:p.Thr572= | |
| ENST00000700417.1:c.1734G>A | ENSP00000514981.1:p.Thr578= | |
| ENST00000700419.1:c.69G>A | ENSP00000514983.1:p.Thr23= | |
| ENST00000700444.1:c.*1575G>A | ENSP00000514992.1:n.*1575G>A | |
| ENST00000303635.12:c.1806G>A MANE Select | ENSP00000306522.6:p.Thr602= | |
| ENST00000303635.11:c.1806G>A | ENSP00000306522.6:p.Thr602= | |
| NM_015215.3:c.1806G>A | NP_056030.1:p.Thr602= | |
| XM_011541083.1:c.1806G>A | XP_011539385.1:p.Thr602= | |
| XM_011541084.1:c.1806G>A | XP_011539386.1:p.Thr602= | |
| XM_011541085.1:c.1794G>A | XP_011539387.1:p.Thr598= | |
| XM_011541086.1:c.1806G>A | XP_011539388.1:p.Thr602= | |
| XM_011541087.1:c.1734G>A | XP_011539389.1:p.Thr578= | |
| XM_011541088.1:c.1716G>A | XP_011539390.1:p.Thr572= | |
| XM_011541089.1:c.1806G>A | XP_011539391.1:p.Thr602= | |
| XM_011541090.1:c.1806G>A | XP_011539392.1:p.Thr602= | |
| XM_011541091.1:c.1806G>A | XP_011539393.1:p.Thr602= | |
| XM_011541092.1:c.1806G>A | XP_011539394.1:p.Thr602= | |
| NM_001349608.1:c.1716G>A | NP_001336537.1:p.Thr572= | |
| NM_001349609.1:c.1806G>A | NP_001336538.1:p.Thr602= | |
| NM_001349610.1:c.1806G>A | NP_001336539.1:p.Thr602= | |
| NM_001349612.1:c.1716G>A | NP_001336541.1:p.Thr572= | |
| XM_011541083.2:c.1806G>A | XP_011539385.1:p.Thr602= | |
| XM_011541084.2:c.1806G>A | XP_011539386.1:p.Thr602= | |
| XM_011541086.3:c.1806G>A | XP_011539388.1:p.Thr602= | |
| XM_011541087.2:c.1734G>A | XP_011539389.1:p.Thr578= | |
| XM_011541088.2:c.1716G>A | XP_011539390.1:p.Thr572= | |
| XM_011541090.3:c.1806G>A | XP_011539392.1:p.Thr602= | |
| XM_011541091.2:c.1806G>A | XP_011539393.1:p.Thr602= | |
| XM_011541092.3:c.1806G>A | XP_011539394.1:p.Thr602= | |
| XM_017000774.2:c.1806G>A | XP_016856263.1:p.Thr602= | |
| XM_017000777.1:c.1806G>A | XP_016856266.1:p.Thr602= | |
| XM_017000778.1:c.1806G>A | XP_016856267.1:p.Thr602= | |
| NM_015215.4:c.1806G>A MANE Select | NP_056030.1:p.Thr602= | |
| NM_001349608.2:c.1716G>A | NP_001336537.1:p.Thr572= | |
| NM_001349609.2:c.1806G>A | NP_001336538.1:p.Thr602= | |
| NM_001349610.2:c.1806G>A | NP_001336539.1:p.Thr602= | |
| NM_001349612.2:c.1716G>A | NP_001336541.1:p.Thr572= |