Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73367787C>A , CM000677.2:g.73367787C>A | GRCh38 |
| NC_000015.9:g.73660128C>A , CM000677.1:g.73660128C>A | GRCh37 |
| NC_000015.8:g.71447181C>A | NCBI36 |
| NG_009063.1:g.6478G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.484G>T MANE Select | ENSP00000261917.3:p.Ala162Ser | |
| ENST00000261917.3:c.484G>T | ENSP00000261917.3:p.Ala162Ser | |
| NM_005477.2:c.484G>T | NP_005468.1:p.Ala162Ser | |
| NM_005477.3:c.484G>T MANE Select | NP_005468.1:p.Ala162Ser |