HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55346115A>T , CM000666.2:g.55346115A>T | GRCh38 |
NC_000004.11:g.56212282A>T , CM000666.1:g.56212282A>T | GRCh37 |
NC_000004.10:g.55907039A>T | NCBI36 |
NG_028230.1:g.4895A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264228.8:c.-222A>T | ENSP00000264228.4:n.-222A>T |