HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271682T>G , CM000668.2:g.31271682T>G | GRCh38 |
NC_000006.11:g.31239459T>G , CM000668.1:g.31239459T>G | GRCh37 |
NC_000006.10:g.31347438T>G | NCBI36 |
NG_029422.2:g.5450A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.260A>C MANE Select | ENSP00000365402.5:p.Glu87Ala | |
ENST00000376228.9:c.260A>C | ENSP00000365402.5:p.Glu87Ala | |
ENST00000376237.8:c.260A>C | ENSP00000365412.4:p.Glu87Ala | |
ENST00000383329.7:c.260A>C | ENSP00000372819.3:p.Glu87Ala | |
ENST00000415537.1:c.258A>C | ||
ENST00000484378.1:n.279A>C | ||
ENST00000487245.5:n.369A>C | ||
ENST00000495835.1:n.449A>C | ||
NM_002117.5:c.260A>C | NP_002108.4:p.Glu87Ala | |
NM_002117.6:c.260A>C MANE Select | NP_002108.4:p.Glu87Ala |