HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269211T>C , CM000668.2:g.31269211T>C | GRCh38 |
NC_000006.11:g.31236988T>C , CM000668.1:g.31236988T>C | GRCh37 |
NC_000006.10:g.31344967T>C | NCBI36 |
NG_029422.2:g.7921A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.1097-38A>G MANE Select | ENSP00000365402.5:n.1097-38A>G | |
ENST00000376228.9:c.1097-38A>G | ENSP00000365402.5:n.1097-38A>G | |
ENST00000376237.8:c.*684-38A>G | ENSP00000365412.4:n.*684-38A>G | |
ENST00000383329.7:c.1115-38A>G | ENSP00000372819.3:n.1115-38A>G | |
ENST00000466892.5:n.330-38A>G | ||
ENST00000470363.5:n.855-38A>G | ||
ENST00000487245.5:n.1456-38A>G | ||
NM_002117.5:c.1097-38A>G | NP_002108.4:n.1097-38A>G | |
NM_002117.6:c.1097-38A>G MANE Select | NP_002108.4:n.1097-38A>G |