Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129532722A= , CM000665.2:g.129532722A= | GRCh38 |
| NC_000003.11:g.129251565A= , CM000665.1:g.129251565A= | GRCh37 |
| NC_000003.10:g.130734255A= | NCBI36 |
| NG_009115.1:g.9084A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000539.3:c.886A= MANE Select | NP_000530.1:p.Lys296= |
| ENST00000296271.4:c.886A= MANE Select | ENSP00000296271.3:p.Lys296= |
| ENST00000296271.3:c.886A= | ENSP00000296271.3:p.Lys296= |