Linked Data
ClinVar Variation Id:
498594
dbSNP Id:
rs148900299
ExAC:
19:10887849 C / T
gnomAD v2:
19-10887849-C-T
gnomAD v3:
19-10777173-C-T
gnomAD v4:
19-10777173-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10777173C>T , CM000681.2:g.10777173C>T | GRCh38 |
| NC_000019.9:g.10887849C>T , CM000681.1:g.10887849C>T | GRCh37 |
| NC_000019.8:g.10748849C>T | NCBI36 |
| NG_008792.1:g.64095C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682285.1:n.833C>T | ||
| ENST00000682524.1:n.833C>T | ||
| ENST00000683738.1:n.833C>T | ||
| ENST00000355667.11:c.645C>T | ENSP00000347890.6:p.Asp215= | |
| ENST00000389253.9:c.645C>T MANE Select | ENSP00000373905.4:p.Asp215= | |
| ENST00000355667.10:c.645C>T | ENSP00000347890.6:p.Asp215= | |
| ENST00000359692.10:c.645C>T | ENSP00000352721.6:p.Asp215= | |
| ENST00000389253.8:c.645C>T | ENSP00000373905.3:p.Asp215= | |
| ENST00000408974.8:c.645C>T | ENSP00000386192.3:p.Asp215= | |
| ENST00000585892.5:c.645C>T | ENSP00000468734.1:p.Asp215= | |
| ENST00000591701.5:n.5C>T | ||
| ENST00000591819.1:n.568C>T | ||
| NM_001005360.2:c.645C>T | NP_001005360.1:p.Asp215= | |
| NM_001005361.2:c.645C>T | NP_001005361.1:p.Asp215= | |
| NM_001005362.2:c.645C>T | NP_001005362.1:p.Asp215= | |
| NM_001190716.1:c.645C>T | NP_001177645.1:p.Asp215= | |
| NM_004945.3:c.645C>T | NP_004936.2:p.Asp215= | |
| NM_001005361.3:c.645C>T MANE Select | NP_001005361.1:p.Asp215= | |
| NM_001190716.2:c.645C>T | NP_001177645.1:p.Asp215= | |
| NM_001005360.3:c.645C>T | NP_001005360.1:p.Asp215= | |
| NM_001005362.3:c.645C>T | NP_001005362.1:p.Asp215= | |
| NM_004945.4:c.645C>T | NP_004936.2:p.Asp215= |