HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269536A>T , CM000668.2:g.31269536A>T | GRCh38 |
NC_000006.11:g.31237313A>T , CM000668.1:g.31237313A>T | GRCh37 |
NC_000006.10:g.31345292A>T | NCBI36 |
NG_029422.2:g.7596T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.1016-11T>A MANE Select | ENSP00000365402.5:n.1016-11T>A | |
ENST00000376228.9:c.1016-11T>A | ENSP00000365402.5:n.1016-11T>A | |
ENST00000376237.8:c.*603-11T>A | ENSP00000365412.4:n.*603-11T>A | |
ENST00000383329.7:c.1023T>A | ENSP00000372819.3:p.Phe341Leu | |
ENST00000466892.5:n.131T>A | ||
ENST00000470363.5:n.763T>A | ||
ENST00000487245.5:n.1375-11T>A | ||
NM_002117.5:c.1016-11T>A | NP_002108.4:n.1016-11T>A | |
NM_002117.6:c.1016-11T>A MANE Select | NP_002108.4:n.1016-11T>A |