Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129531016G= , CM000665.2:g.129531016G= | GRCh38 |
| NC_000003.11:g.129249859G= , CM000665.1:g.129249859G= | GRCh37 |
| NC_000003.10:g.130732549G= | NCBI36 |
| NG_009115.1:g.7378G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.502G= MANE Select | ENSP00000296271.3:p.Ala168= | |
| ENST00000296271.3:c.502G= | ENSP00000296271.3:p.Ala168= | |
| NM_000539.3:c.502G= MANE Select | NP_000530.1:p.Ala168= |