Linked Data
ClinVar Variation Id:
2028719
ClinVar RCV Id:
RCV002876279
dbSNP Id:
rs1379630288
MyVariant Identifiers:
chr19:g.1206936G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1206937G>A , CM000681.2:g.1206937G>A | GRCh38 |
| NC_000019.9:g.1206936G>A , CM000681.1:g.1206936G>A | GRCh37 |
| NC_000019.8:g.1157936G>A | NCBI36 |
| NG_007460.2:g.22531G>A , LRG_319:g.22531G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.24G>A | ENSP00000490268.2:p.Gln8= | |
| ENST00000585748.3:c.-82-11480G>A | ENSP00000477641.2:n.-82-11480G>A | |
| ENST00000585851.2:c.24G>A | ENSP00000467912.2:p.Gln8= | |
| ENST00000326873.12:c.24G>A MANE Select | ENSP00000324856.6:p.Gln8= | |
| ENST00000652231.1:c.24G>A | ENSP00000498804.1:p.Gln8= | |
| ENST00000326873.11:c.24G>A | ENSP00000324856.6:p.Gln8= | |
| ENST00000585748.2:c.-82-11480G>A | ENSP00000477641.1:n.-82-11480G>A | |
| ENST00000585851.1:c.24G>A | ENSP00000467912.1:p.Gln8= | |
| ENST00000586243.5:c.24G>A | ENSP00000467240.2:p.Gln8= | |
| ENST00000589152.5:n.114G>A | ||
| ENST00000593219.5:c.24G>A | ENSP00000466610.1:p.Gln8= | |
| NM_000455.4:c.24G>A , LRG_319t1:c.24G>A | NP_000446.1:p.Gln8= | |
| XM_005259617.1:c.24G>A | XP_005259674.1:p.Gln8= | |
| XM_005259618.3:c.24G>A | XP_005259675.1:p.Gln8= | |
| XM_011528209.1:c.-330G>A | XP_011526511.1:n.-330G>A | |
| XR_936204.1:n.649G>A | ||
| XM_005259617.3:c.24G>A | XP_005259674.1:p.Gln8= | |
| XM_011528209.2:c.-330G>A | XP_011526511.1:n.-330G>A | |
| XR_001753738.2:n.649G>A | ||
| XR_001753739.1:n.649G>A | ||
| XR_001753740.2:n.649G>A | ||
| NM_000455.5:c.24G>A MANE Select | NP_000446.1:p.Gln8= |