HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133353788C>G , CM000671.2:g.133353788C>G | GRCh38 |
NC_000009.10:g.135210464C>G | NCBI36 |
NG_008477.1:g.7719G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371974.8:c.476G>C MANE Select | ENSP00000361042.3:p.Gly159Ala | |
ENST00000371974.7:c.476G>C | ENSP00000361042.3:p.Gly159Ala | |
ENST00000437995.1:n.422G>C | ||
ENST00000495952.5:n.466G>C | ||
ENST00000615505.4:c.149G>C | ENSP00000482067.1:p.Gly50Ala | |
NM_001280787.1:c.149G>C | NP_001267716.1:p.Gly50Ala | |
NM_003172.3:c.476G>C | NP_003163.1:p.Gly159Ala | |
XM_011518942.1:c.149G>C | XP_011517244.1:p.Gly50Ala | |
NM_003172.4:c.476G>C MANE Select | NP_003163.1:p.Gly159Ala |