HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131851239C>G , CM000668.2:g.131851239C>G | GRCh38 |
NC_000006.11:g.132172379C>G , CM000668.1:g.132172379C>G | GRCh37 |
NC_000006.10:g.132214072C>G | NCBI36 |
NG_008206.1:g.48224C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647893.1:c.528C>G MANE Select | ENSP00000498074.1:p.Cys176Trp | |
ENST00000650147.1:c.206C>G | ||
ENST00000650437.1:c.108+1133C>G | ||
ENST00000360971.6:c.528C>G | ENSP00000354238.2:p.Cys176Trp | |
ENST00000486853.1:n.548C>G | ||
ENST00000513998.5:c.528C>G | ENSP00000422424.1:p.Cys176Trp | |
NM_006208.2:c.528C>G | NP_006199.2:p.Cys176Trp | |
NM_006208.3:c.528C>G MANE Select | NP_006199.2:p.Cys176Trp |