HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269496C>T , CM000668.2:g.31269496C>T | GRCh38 |
NC_000006.11:g.31237273C>T , CM000668.1:g.31237273C>T | GRCh37 |
NC_000006.10:g.31345252C>T | NCBI36 |
NG_029422.2:g.7636G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.1045G>A MANE Select | ENSP00000365402.5:p.Ala349Thr | |
ENST00000376228.9:c.1045G>A | ENSP00000365402.5:p.Ala349Thr | |
ENST00000376237.8:c.*632G>A | ENSP00000365412.4:n.*632G>A | |
ENST00000383329.7:c.1063G>A | ENSP00000372819.3:p.Ala355Thr | |
ENST00000466892.5:n.171G>A | ||
ENST00000470363.5:n.803G>A | ||
ENST00000487245.5:n.1404G>A | ||
NM_002117.5:c.1045G>A | NP_002108.4:p.Ala349Thr | |
NM_002117.6:c.1045G>A MANE Select | NP_002108.4:p.Ala349Thr |