Linked Data
ClinVar Variation Id:
7456
ClinVar RCV Id:
RCV000007882
dbSNP Id:
rs137853080
PubMed:
PMID:10201537
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1207058T>G , CM000681.2:g.1207058T>G | GRCh38 |
| NC_000019.9:g.1207057T>G , CM000681.1:g.1207057T>G | GRCh37 |
| NC_000019.8:g.1158057T>G | NCBI36 |
| NG_007460.2:g.22652T>G , LRG_319:g.22652T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000585465.3:c.145T>G | ENSP00000490268.2:p.Tyr49Asp | |
| ENST00000585748.3:c.-82-11359T>G | ENSP00000477641.2:n.-82-11359T>G | |
| ENST00000585851.2:c.145T>G | ENSP00000467912.2:p.Tyr49Asp | |
| ENST00000326873.12:c.145T>G MANE Select | ENSP00000324856.6:p.Tyr49Asp | |
| ENST00000652231.1:c.145T>G | ENSP00000498804.1:p.Tyr49Asp | |
| ENST00000326873.11:c.145T>G | ENSP00000324856.6:p.Tyr49Asp | |
| ENST00000585748.2:c.-82-11359T>G | ENSP00000477641.1:n.-82-11359T>G | |
| ENST00000585851.1:c.145T>G | ENSP00000467912.1:p.Tyr49Asp | |
| ENST00000586243.5:c.145T>G | ENSP00000467240.2:p.Tyr49Asp | |
| ENST00000589152.5:n.235T>G | ||
| ENST00000593219.5:c.145T>G | ENSP00000466610.1:p.Tyr49Asp | |
| NM_000455.4:c.145T>G , LRG_319t1:c.145T>G | NP_000446.1:p.Tyr49Asp | |
| XM_005259617.1:c.145T>G | XP_005259674.1:p.Tyr49Asp | |
| XM_005259618.3:c.145T>G | XP_005259675.1:p.Tyr49Asp | |
| XM_011528209.1:c.-209T>G | XP_011526511.1:n.-209T>G | |
| XR_936204.1:n.770T>G | ||
| XM_005259617.3:c.145T>G | XP_005259674.1:p.Tyr49Asp | |
| XM_011528209.2:c.-209T>G | XP_011526511.1:n.-209T>G | |
| XR_001753738.2:n.770T>G | ||
| XR_001753739.1:n.770T>G | ||
| XR_001753740.2:n.770T>G | ||
| NM_000455.5:c.145T>G MANE Select | NP_000446.1:p.Tyr49Asp |