HGVS | Genome Assembly |
---|---|
NC_000017.11:g.56594799C>T , CM000679.2:g.56594799C>T | GRCh38 |
NC_000017.10:g.54672160C>T , CM000679.1:g.54672160C>T | GRCh37 |
NC_000017.9:g.52027159C>T | NCBI36 |
NG_011958.1:g.6101C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000332822.6:c.576C>T MANE Select | ENSP00000328181.4:p.Cys192= | |
ENST00000332822.4:c.576C>T | ENSP00000328181.4:p.Cys192= | |
NM_005450.4:c.576C>T | NP_005441.1:p.Cys192= | |
NM_005450.6:c.576C>T MANE Select | NP_005441.1:p.Cys192= |