Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55346188T>G , CM000666.2:g.55346188T>G | GRCh38 |
| NC_000004.11:g.56212355T>G , CM000666.1:g.56212355T>G | GRCh37 |
| NC_000004.10:g.55907112T>G | NCBI36 |
| NG_028230.1:g.4968T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264228.8:c.-149T>G | ENSP00000264228.4:n.-149T>G |