Linked Data
ClinVar Variation Id:
1451892
ClinVar RCV Id:
RCV002007444
dbSNP Id:
rs2145436556
gnomAD v4:
19-1226620-C-T
MyVariant Identifiers:
chr19:g.1226619C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1226620C>T , CM000681.2:g.1226620C>T | GRCh38 |
| NC_000019.9:g.1226619C>T , CM000681.1:g.1226619C>T | GRCh37 |
| NC_000019.8:g.1177619C>T | NCBI36 |
| NG_007460.2:g.42214C>T , LRG_319:g.42214C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.*2876C>T | ENSP00000490268.2:n.*2876C>T | |
| ENST00000585748.3:c.903C>T | ENSP00000477641.2:p.Arg301= | |
| ENST00000585851.2:c.1101C>T | ENSP00000467912.2:p.Arg367= | |
| ENST00000326873.12:c.1275C>T MANE Select | ENSP00000324856.6:p.Arg425= | |
| ENST00000326873.11:c.1275C>T | ENSP00000324856.6:p.Arg425= | |
| ENST00000585465.2:n.3008C>T | ||
| ENST00000586243.5:c.1272C>T | ENSP00000467240.2:p.Arg424= | |
| ENST00000589152.5:n.1973C>T | ||
| NM_000455.4:c.1275C>T , LRG_319t1:c.1275C>T | NP_000446.1:p.Arg425= | |
| XM_005259617.1:c.1270C>T | XP_005259674.1:p.Pro424Ser | |
| XM_011528209.1:c.1048C>T | XP_011526511.1:p.Pro350Ser | |
| XM_005259617.3:c.1270C>T | XP_005259674.1:p.Pro424Ser | |
| XM_011528209.2:c.1048C>T | XP_011526511.1:p.Pro350Ser | |
| XR_001753738.2:n.2081C>T | ||
| XR_001753740.2:n.2051C>T | ||
| NM_000455.5:c.1275C>T MANE Select | NP_000446.1:p.Arg425= |