HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269007G= , CM000668.2:g.31269007G= | GRCh38 |
NC_000006.11:g.31236784G= , CM000668.1:g.31236784G= | GRCh37 |
NC_000006.10:g.31344763G= | NCBI36 |
NG_029422.2:g.8125C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.*162C= MANE Select | ENSP00000365402.5:n.*162C= | |
ENST00000376228.9:c.*162C= | ENSP00000365402.5:n.*162C= | |
ENST00000376237.8:c.*850C= | ENSP00000365412.4:n.*850C= | |
ENST00000383329.7:c.*162C= | ENSP00000372819.3:n.*162C= | |
ENST00000466892.5:n.496C= | ||
ENST00000470363.5:n.1021C= | ||
ENST00000487245.5:n.1622C= | ||
NM_002117.5:c.*162C= | NP_002108.4:n.*162C= | |
NM_002117.6:c.*162C= MANE Select | NP_002108.4:n.*162C= |