HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269063C>A , CM000668.2:g.31269063C>A | GRCh38 |
NC_000006.11:g.31236840C>A , CM000668.1:g.31236840C>A | GRCh37 |
NC_000006.10:g.31344819C>A | NCBI36 |
NG_029422.2:g.8069G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.*106G>T MANE Select | ENSP00000365402.5:n.*106G>T | |
ENST00000376228.9:c.*106G>T | ENSP00000365402.5:n.*106G>T | |
ENST00000376237.8:c.*794G>T | ENSP00000365412.4:n.*794G>T | |
ENST00000383329.7:c.*106G>T | ENSP00000372819.3:n.*106G>T | |
ENST00000466892.5:n.440G>T | ||
ENST00000470363.5:n.965G>T | ||
ENST00000487245.5:n.1566G>T | ||
NM_002117.5:c.*106G>T | NP_002108.4:n.*106G>T | |
NM_002117.6:c.*106G>T MANE Select | NP_002108.4:n.*106G>T |