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