Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155463312T>A , CM000669.2:g.155463312T>A | GRCh38 |
| NC_000007.13:g.155256007T>A , CM000669.1:g.155256007T>A | GRCh37 |
| NC_000007.12:g.154948768T>A | NCBI36 |
| NG_007124.1:g.11593T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297375.4:c.*625T>A MANE Select | ENSP00000297375.4:n.*625T>A | |
| NM_001427.3:c.*625T>A | NP_001418.2:n.*625T>A | |
| NM_001427.4:c.*625T>A MANE Select | NP_001418.2:n.*625T>A |