Linked Data
ClinVar Variation Id:
184047
dbSNP Id:
rs369033659
ExAC:
19:1226603 C / T
gnomAD v2:
19-1226603-C-T
gnomAD v4:
19-1226604-C-T
MyVariant Identifiers:
chr19:g.1226603C>T (hg19)
chr19:g.1226603_1226606delinsTCAG (hg19)
chr19:g.1226604C>T (hg38)
PubMed:
PMID:19145097
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1226604C>T , CM000681.2:g.1226604C>T | GRCh38 |
| NC_000019.9:g.1226603C>T , CM000681.1:g.1226603C>T | GRCh37 |
| NC_000019.8:g.1177603C>T | NCBI36 |
| NG_007460.2:g.42198C>T , LRG_319:g.42198C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.*2860C>T | ENSP00000490268.2:n.*2860C>T | |
| ENST00000585748.3:c.887C>T | ENSP00000477641.2:p.Ala296Val | |
| ENST00000585851.2:c.1085C>T | ENSP00000467912.2:p.Ala362Val | |
| ENST00000326873.12:c.1259C>T MANE Select | ENSP00000324856.6:p.Ala420Val | |
| ENST00000326873.11:c.1259C>T | ENSP00000324856.6:p.Ala420Val | |
| ENST00000585465.2:n.2992C>T | ||
| ENST00000586243.5:c.1256C>T | ENSP00000467240.2:p.Ala419Val | |
| ENST00000589152.5:n.1957C>T | ||
| NM_000455.4:c.1259C>T , LRG_319t1:c.1259C>T | NP_000446.1:p.Ala420Val | |
| XM_005259617.1:c.1254C>T | XP_005259674.1:p.Arg418= | |
| XM_011528209.1:c.1032C>T | XP_011526511.1:p.Arg344= | |
| XM_005259617.3:c.1254C>T | XP_005259674.1:p.Arg418= | |
| XM_011528209.2:c.1032C>T | XP_011526511.1:p.Arg344= | |
| XR_001753738.2:n.2065C>T | ||
| XR_001753740.2:n.2035C>T | ||
| NM_000455.5:c.1259C>T MANE Select | NP_000446.1:p.Ala420Val |