HGVS | Genome Assembly |
---|---|
NC_000010.11:g.80275081T>G , CM000672.2:g.80275081T>G | GRCh38 |
NC_000010.10:g.82034837T>G , CM000672.1:g.82034837T>G | GRCh37 |
NC_000010.9:g.82024817T>G | NCBI36 |
NG_008083.1:g.19598A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372213.8:c.887A>C MANE Select | ENSP00000361287.3:p.Tyr296Ser | |
ENST00000372213.7:c.887A>C | ENSP00000361287.3:p.Tyr296Ser | |
ENST00000480845.1:n.119A>C | ||
ENST00000485270.5:n.399A>C | ||
NM_000429.2:c.887A>C | NP_000420.1:p.Tyr296Ser | |
XM_005269842.3:c.887A>C | XP_005269899.1:p.Tyr296Ser | |
XM_005269843.3:c.764A>C | XP_005269900.1:p.Tyr255Ser | |
NM_000429.3:c.887A>C MANE Select | NP_000420.1:p.Tyr296Ser |