Linked Data
ClinVar Variation Id:
1143896
ClinVar RCV Id:
RCV001482191
dbSNP Id:
rs786201509
MyVariant Identifiers:
chr19:g.1220609C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1220610C>A , CM000681.2:g.1220610C>A | GRCh38 |
| NC_000019.9:g.1220609C>A , CM000681.1:g.1220609C>A | GRCh37 |
| NC_000019.8:g.1171609C>A | NCBI36 |
| NG_007460.2:g.36204C>A , LRG_319:g.36204C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.627C>A | ENSP00000490268.2:p.Thr209= | |
| ENST00000585748.3:c.255C>A | ENSP00000477641.2:p.Thr85= | |
| ENST00000585851.2:c.453C>A | ENSP00000467912.2:p.Thr151= | |
| ENST00000326873.12:c.627C>A MANE Select | ENSP00000324856.6:p.Thr209= | |
| ENST00000652231.1:c.627C>A | ENSP00000498804.1:p.Thr209= | |
| ENST00000326873.11:c.627C>A | ENSP00000324856.6:p.Thr209= | |
| ENST00000585851.1:c.453C>A | ENSP00000467912.1:p.Thr151= | |
| ENST00000586243.5:c.627C>A | ENSP00000467240.2:p.Thr209= | |
| ENST00000586358.5:n.525C>A | ||
| ENST00000589152.5:n.717C>A | ||
| ENST00000591133.2:n.598C>A | ||
| NM_000455.4:c.627C>A , LRG_319t1:c.627C>A | NP_000446.1:p.Thr209= | |
| XM_005259617.1:c.627C>A | XP_005259674.1:p.Thr209= | |
| XM_005259618.3:c.627C>A | XP_005259675.1:p.Thr209= | |
| XM_011528209.1:c.405C>A | XP_011526511.1:p.Thr135= | |
| XR_936204.1:n.1252C>A | ||
| XM_005259617.3:c.627C>A | XP_005259674.1:p.Thr209= | |
| XM_011528209.2:c.405C>A | XP_011526511.1:p.Thr135= | |
| XR_001753738.2:n.1252C>A | ||
| XR_001753739.1:n.1252C>A | ||
| XR_001753740.2:n.1252C>A | ||
| NM_000455.5:c.627C>A MANE Select | NP_000446.1:p.Thr209= |