HGVS | Genome Assembly |
---|---|
NC_000010.11:g.80275154C>T , CM000672.2:g.80275154C>T | GRCh38 |
NC_000010.10:g.82034910C>T , CM000672.1:g.82034910C>T | GRCh37 |
NC_000010.9:g.82024890C>T | NCBI36 |
NG_008083.1:g.19525G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372213.8:c.814G>A MANE Select | ENSP00000361287.3:p.Gly272Ser | |
ENST00000372213.7:c.814G>A | ENSP00000361287.3:p.Gly272Ser | |
ENST00000480845.1:n.46G>A | ||
ENST00000485270.5:n.326G>A | ||
NM_000429.2:c.814G>A | NP_000420.1:p.Gly272Ser | |
XM_005269842.3:c.814G>A | XP_005269899.1:p.Gly272Ser | |
XM_005269843.3:c.691G>A | XP_005269900.1:p.Gly231Ser | |
NM_000429.3:c.814G>A MANE Select | NP_000420.1:p.Gly272Ser |