HGVS | Genome Assembly |
---|---|
NC_000004.12:g.119320713C>T , CM000666.2:g.119320713C>T | GRCh38 |
NC_000004.11:g.120241868C>T , CM000666.1:g.120241868C>T | GRCh37 |
NC_000004.10:g.120461316C>T | NCBI36 |
NG_011444.1:g.6449G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274024.4:c.197G>A MANE Select | ENSP00000274024.3:p.Gly66Asp | |
ENST00000274024.3:c.197G>A | ENSP00000274024.3:p.Gly66Asp | |
NM_000134.3:c.197G>A | NP_000125.2:p.Gly66Asp | |
NM_000134.4:c.197G>A MANE Select | NP_000125.2:p.Gly66Asp |