HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269002G= , CM000668.2:g.31269002G= | GRCh38 |
NC_000006.11:g.31236779G= , CM000668.1:g.31236779G= | GRCh37 |
NC_000006.10:g.31344758G= | NCBI36 |
NG_029422.2:g.8130C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.*167C= MANE Select | ENSP00000365402.5:n.*167C= | |
ENST00000376228.9:c.*167C= | ENSP00000365402.5:n.*167C= | |
ENST00000376237.8:c.*855C= | ENSP00000365412.4:n.*855C= | |
ENST00000383329.7:c.*167C= | ENSP00000372819.3:n.*167C= | |
ENST00000466892.5:n.501C= | ||
ENST00000470363.5:n.1026C= | ||
ENST00000487245.5:n.1627C= | ||
NM_002117.5:c.*167C= | NP_002108.4:n.*167C= | |
NM_002117.6:c.*167C= MANE Select | NP_002108.4:n.*167C= |