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