Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129532521C= , CM000665.2:g.129532521C= | GRCh38 |
| NC_000003.11:g.129251364C= , CM000665.1:g.129251364C= | GRCh37 |
| NC_000003.10:g.130734054C= | NCBI36 |
| NG_009115.1:g.8883C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296271.4:c.697-12C= MANE Select | ENSP00000296271.3:n.697-12C= | |
| ENST00000296271.3:c.697-12C= | ENSP00000296271.3:n.697-12C= | |
| NM_000539.3:c.697-12C= MANE Select | NP_000530.1:n.697-12C= |