HGVS | Genome Assembly |
---|---|
NC_000006.12:g.53922787T>G , CM000668.2:g.53922787T>G | GRCh38 |
NC_000006.11:g.53787585T>G , CM000668.1:g.53787585T>G | GRCh37 |
NC_000006.10:g.53895544T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370888.6:c.1569T>G MANE Select | ENSP00000359925.1:p.Ser523= | |
ENST00000370888.5:c.1569T>G | ENSP00000359925.1:p.Ser523= | |
NM_018214.4:c.1569T>G | NP_060684.4:p.Ser523= | |
XM_011514726.1:c.1569T>G | XP_011513028.1:p.Ser523= | |
XM_011514727.1:c.1392T>G | XP_011513029.1:p.Ser464= | |
XM_011514726.2:c.1569T>G | XP_011513028.1:p.Ser523= | |
XM_011514727.2:c.1392T>G | XP_011513029.1:p.Ser464= | |
XR_001743504.1:n.2207T>G | ||
NM_018214.5:c.1569T>G MANE Select | NP_060684.4:p.Ser523= |