HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10673527G= , CM000682.2:g.10673527G= | GRCh38 |
NC_000020.10:g.10654175G= , CM000682.1:g.10654175G= | GRCh37 |
NC_000020.9:g.10602175G= | NCBI36 |
NG_007496.1:g.5520C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.4C= MANE Select | ENSP00000254958.4:p.Arg2= | |
ENST00000254958.9:c.4C= | ENSP00000254958.4:p.Arg2= | |
NM_000214.2:c.4C= | NP_000205.1:p.Arg2= | |
NM_000214.3:c.4C= MANE Select | NP_000205.1:p.Arg2= |