Linked Data
dbSNP Id:
rs1179584499
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4911979A>G , CM000674.2:g.4911979A>G | GRCh38 |
| NC_000012.11:g.5021145A>G , CM000674.1:g.5021145A>G | GRCh37 |
| NC_000012.10:g.4891406A>G | NCBI36 |
| NG_011815.1:g.7073A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.601A>G MANE Select | ENSP00000371985.3:p.Thr201Ala | |
| ENST00000543874.3:n.105+1507A>G | ||
| ENST00000639306.1:c.439A>G | ENSP00000492506.1:p.Thr147Ala | |
| ENST00000382545.3:c.601A>G | ENSP00000371985.3:p.Thr201Ala | |
| ENST00000541095.1:n.105+1507A>G | ||
| ENST00000543874.2:n.96+1507A>G | ||
| NM_000217.2:c.601A>G | NP_000208.2:p.Thr201Ala | |
| NM_000217.3:c.601A>G MANE Select | NP_000208.2:p.Thr201Ala |