HGVS | Genome Assembly |
---|---|
NC_000004.12:g.119320740C= , CM000666.2:g.119320740C= | GRCh38 |
NC_000004.11:g.120241895C= , CM000666.1:g.120241895C= | GRCh37 |
NC_000004.10:g.120461343C= | NCBI36 |
NG_011444.1:g.6422G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274024.4:c.170G= MANE Select | ENSP00000274024.3:p.Arg57= | |
ENST00000274024.3:c.170G= | ENSP00000274024.3:p.Arg57= | |
NM_000134.3:c.170G= | NP_000125.2:p.Arg57= | |
NM_000134.4:c.170G= MANE Select | NP_000125.2:p.Arg57= |