Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149928122C>A , CM000663.2:g.149928122C>A | GRCh38 |
| NC_000001.10:g.149900014C>A , CM000663.1:g.149900014C>A | GRCh37 |
| NC_000001.9:g.148166638C>A | NCBI36 |
| NG_032777.1:g.5131G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.8:c.-363G>T | ENSP00000271628.8:n.-363G>T | |
| NM_005850.4:c.-363G>T | NP_005841.1:n.-363G>T |