HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269091G= , CM000668.2:g.31269091G= | GRCh38 |
NC_000006.11:g.31236868G= , CM000668.1:g.31236868G= | GRCh37 |
NC_000006.10:g.31344847G= | NCBI36 |
NG_029422.2:g.8041C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.*78C= MANE Select | ENSP00000365402.5:n.*78C= | |
ENST00000376228.9:c.*78C= | ENSP00000365402.5:n.*78C= | |
ENST00000376237.8:c.*766C= | ENSP00000365412.4:n.*766C= | |
ENST00000383329.7:c.*78C= | ENSP00000372819.3:n.*78C= | |
ENST00000466892.5:n.412C= | ||
ENST00000470363.5:n.937C= | ||
ENST00000487245.5:n.1538C= | ||
NM_002117.5:c.*78C= | NP_002108.4:n.*78C= | |
NM_002117.6:c.*78C= MANE Select | NP_002108.4:n.*78C= |