Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55008508G>A , CM000663.2:g.55008508G>A | GRCh38 |
| NC_000001.10:g.55474181G>A , CM000663.1:g.55474181G>A | GRCh37 |
| NC_000001.9:g.55246769G>A | NCBI36 |
| NG_008965.1:g.14565G>A | |
| NG_008965.2:g.14576G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_057176.3:c.843G>A MANE Select | NP_476517.1:p.Ser281= |
| ENST00000651561.1:c.843G>A MANE Select | ENSP00000498282.1:p.Ser281= |
| NM_057176.2:c.843G>A | NP_476517.1:p.Ser281= |
| ENST00000371265.4:c.843G>A | ENSP00000360312.4:p.Ser281= |
| XM_006710883.2:c.612G>A | XP_006710946.1:p.Ser204= |