HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55346198G>T , CM000666.2:g.55346198G>T | GRCh38 |
NC_000004.11:g.56212365G>T , CM000666.1:g.56212365G>T | GRCh37 |
NC_000004.10:g.55907122G>T | NCBI36 |
NG_028230.1:g.4978G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264228.8:c.-139G>T | ENSP00000264228.4:n.-139G>T |