HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269358T>G , CM000668.2:g.31269358T>G | GRCh38 |
NC_000006.11:g.31237135T>G , CM000668.1:g.31237135T>G | GRCh37 |
NC_000006.10:g.31345114T>G | NCBI36 |
NG_029422.2:g.7774A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.1076A>C MANE Select | ENSP00000365402.5:p.Glu359Ala | |
ENST00000376228.9:c.1076A>C | ENSP00000365402.5:p.Glu359Ala | |
ENST00000376237.8:c.*663A>C | ENSP00000365412.4:n.*663A>C | |
ENST00000383329.7:c.1094A>C | ENSP00000372819.3:p.Glu365Ala | |
ENST00000466892.5:n.309A>C | ||
ENST00000470363.5:n.834A>C | ||
ENST00000487245.5:n.1435A>C | ||
NM_002117.5:c.1076A>C | NP_002108.4:p.Glu359Ala | |
NM_002117.6:c.1076A>C MANE Select | NP_002108.4:p.Glu359Ala |