HGVS | Genome Assembly |
---|---|
NC_000019.10:g.41018075C= , CM000681.2:g.41018075C= | GRCh38 |
NC_000019.9:g.41523980C= , CM000681.1:g.41523980C= | GRCh37 |
NC_000019.8:g.46215820C= | NCBI36 |
NG_007929.1:g.31777C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000324071.10:c.*1248C= MANE Select | ENSP00000324648.2:n.*1248C= | |
ENST00000324071.8:c.*1248C= | ENSP00000324648.2:n.*1248C= | |
NM_000767.4:c.*1248C= | NP_000758.1:n.*1248C= | |
XM_011526548.1:c.*1248C= | XP_011524850.1:n.*1248C= | |
XM_011526549.1:c.*1248C= | XP_011524851.1:n.*1248C= | |
XM_011526550.1:c.*1248C= | XP_011524852.1:n.*1248C= | |
NM_000767.5:c.*1248C= MANE Select | NP_000758.1:n.*1248C= |