Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.139963206T= , CM000665.2:g.139963206T= | GRCh38 |
| NC_000003.11:g.139682048T= , CM000665.1:g.139682048T= | GRCh37 |
| NC_000003.10:g.141164738T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022131.3:c.109+27723T= MANE Select | NP_071414.2:n.109+27723T= |
| ENST00000458420.7:c.109+27723T= MANE Select | ENSP00000402460.2:n.109+27723T= |
| NM_022131.2:c.109+27723T= | NP_071414.2:n.109+27723T= |
| ENST00000511524.1:n.297+27723T= |