Linked Data
ClinVar Variation Id:
1733189
ClinVar RCV Id:
RCV002455302
dbSNP Id:
rs2080758985
MyVariant Identifiers:
chr19:g.1218485A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1218486A>G , CM000681.2:g.1218486A>G | GRCh38 |
| NC_000019.9:g.1218485A>G , CM000681.1:g.1218485A>G | GRCh37 |
| NC_000019.8:g.1169485A>G | NCBI36 |
| NG_007460.2:g.34080A>G , LRG_319:g.34080A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.360A>G | ENSP00000490268.2:p.Glu120= | |
| ENST00000585748.3:c.-13A>G | ENSP00000477641.2:n.-13A>G | |
| ENST00000585851.2:c.291-1887A>G | ENSP00000467912.2:n.291-1887A>G | |
| ENST00000326873.12:c.360A>G MANE Select | ENSP00000324856.6:p.Glu120= | |
| ENST00000652231.1:c.360A>G | ENSP00000498804.1:p.Glu120= | |
| ENST00000326873.11:c.360A>G | ENSP00000324856.6:p.Glu120= | |
| ENST00000585748.2:c.-13A>G | ENSP00000477641.1:n.-13A>G | |
| ENST00000585851.1:c.291-1887A>G | ENSP00000467912.1:n.291-1887A>G | |
| ENST00000586243.5:c.360A>G | ENSP00000467240.2:p.Glu120= | |
| ENST00000586358.5:n.183A>G | ||
| ENST00000589152.5:n.450A>G | ||
| ENST00000593219.5:c.*185A>G | ENSP00000466610.1:n.*185A>G | |
| NM_000455.4:c.360A>G , LRG_319t1:c.360A>G | NP_000446.1:p.Glu120= | |
| XM_005259617.1:c.360A>G | XP_005259674.1:p.Glu120= | |
| XM_005259618.3:c.360A>G | XP_005259675.1:p.Glu120= | |
| XM_011528209.1:c.138A>G | XP_011526511.1:p.Glu46= | |
| XR_936204.1:n.985A>G | ||
| XM_005259617.3:c.360A>G | XP_005259674.1:p.Glu120= | |
| XM_011528209.2:c.138A>G | XP_011526511.1:p.Glu46= | |
| XR_001753738.2:n.985A>G | ||
| XR_001753739.1:n.985A>G | ||
| XR_001753740.2:n.985A>G | ||
| NM_000455.5:c.360A>G MANE Select | NP_000446.1:p.Glu120= |