HGVS | Genome Assembly |
---|---|
NC_000005.10:g.146339879C= , CM000667.2:g.146339879C= | GRCh38 |
NC_000005.9:g.145719442C= , CM000667.1:g.145719442C= | GRCh37 |
NC_000005.8:g.145699635C= | NCBI36 |
NG_011885.1:g.5856C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000646991.2:c.452C= MANE Select | ENSP00000495718.1:p.Ala151= | |
ENST00000230732.4:c.452C= | ENSP00000230732.4:p.Ala151= | |
NM_002700.2:c.452C= | NP_002691.1:p.Ala151= | |
NM_002700.3:c.452C= MANE Select | NP_002691.1:p.Ala151= |