HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55346164G>C , CM000666.2:g.55346164G>C | GRCh38 |
NC_000004.11:g.56212331G>C , CM000666.1:g.56212331G>C | GRCh37 |
NC_000004.10:g.55907088G>C | NCBI36 |
NG_028230.1:g.4944G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264228.8:c.-173G>C | ENSP00000264228.4:n.-173G>C |