HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269144T= , CM000668.2:g.31269144T= | GRCh38 |
NC_000006.11:g.31236921T= , CM000668.1:g.31236921T= | GRCh37 |
NC_000006.10:g.31344900T= | NCBI36 |
NG_029422.2:g.7988A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.*25A= MANE Select | ENSP00000365402.5:n.*25A= | |
ENST00000376228.9:c.*25A= | ENSP00000365402.5:n.*25A= | |
ENST00000376237.8:c.*713A= | ENSP00000365412.4:n.*713A= | |
ENST00000383329.7:c.*25A= | ENSP00000372819.3:n.*25A= | |
ENST00000466892.5:n.359A= | ||
ENST00000470363.5:n.884A= | ||
ENST00000487245.5:n.1485A= | ||
NM_002117.5:c.*25A= | NP_002108.4:n.*25A= | |
NM_002117.6:c.*25A= MANE Select | NP_002108.4:n.*25A= |