HGVS | Genome Assembly |
---|---|
NC_000010.11:g.80275133C>A , CM000672.2:g.80275133C>A | GRCh38 |
NC_000010.10:g.82034889C>A , CM000672.1:g.82034889C>A | GRCh37 |
NC_000010.9:g.82024869C>A | NCBI36 |
NG_008083.1:g.19546G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372213.8:c.835G>T MANE Select | ENSP00000361287.3:p.Gly279Cys | |
ENST00000372213.7:c.835G>T | ENSP00000361287.3:p.Gly279Cys | |
ENST00000480845.1:n.67G>T | ||
ENST00000485270.5:n.347G>T | ||
NM_000429.2:c.835G>T | NP_000420.1:p.Gly279Cys | |
XM_005269842.3:c.835G>T | XP_005269899.1:p.Gly279Cys | |
XM_005269843.3:c.712G>T | XP_005269900.1:p.Gly238Cys | |
NM_000429.3:c.835G>T MANE Select | NP_000420.1:p.Gly279Cys |