HGVS | Genome Assembly |
---|---|
NC_000017.11:g.63940997C>A , CM000679.2:g.63940997C>A | GRCh38 |
NC_000017.10:g.62018357C>A , CM000679.1:g.62018357C>A | GRCh37 |
NC_000017.9:g.59372089C>A | NCBI36 |
NG_011699.1:g.36922G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000435607.3:c.5285G>T MANE Select | ENSP00000396320.1:p.Gly1762Val | |
ENST00000578147.5:c.5285G>T | ENSP00000463963.1:p.Gly1762Val | |
NM_000334.4:c.5285G>T MANE Select | NP_000325.4:p.Gly1762Val | |
XM_005257566.3:c.5285G>T | XP_005257623.1:p.Gly1762Val |