Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4912198G>T , CM000674.2:g.4912198G>T | GRCh38 |
| NC_000012.11:g.5021364G>T , CM000674.1:g.5021364G>T | GRCh37 |
| NC_000012.10:g.4891625G>T | NCBI36 |
| NG_011815.1:g.7292G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.820G>T MANE Select | ENSP00000371985.3:p.Ala274Ser | |
| ENST00000543874.3:n.105+1726G>T | ||
| ENST00000639306.1:c.658G>T | ENSP00000492506.1:p.Ala220Ser | |
| ENST00000639680.1:c.8G>T | ||
| ENST00000382545.3:c.820G>T | ENSP00000371985.3:p.Ala274Ser | |
| ENST00000541095.1:n.105+1726G>T | ||
| ENST00000543874.2:n.96+1726G>T | ||
| NM_000217.2:c.820G>T | NP_000208.2:p.Ala274Ser | |
| NM_000217.3:c.820G>T MANE Select | NP_000208.2:p.Ala274Ser |