HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31270351T>C , CM000668.2:g.31270351T>C | GRCh38 |
NC_000006.11:g.31238128T>C , CM000668.1:g.31238128T>C | GRCh37 |
NC_000006.10:g.31346107T>C | NCBI36 |
NG_029422.2:g.6781A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.754A>G MANE Select | ENSP00000365402.5:p.Thr252Ala | |
ENST00000376228.9:c.754A>G | ENSP00000365402.5:p.Thr252Ala | |
ENST00000376237.8:c.*341A>G | ENSP00000365412.4:n.*341A>G | |
ENST00000383329.7:c.754A>G | ENSP00000372819.3:p.Thr252Ala | |
ENST00000415537.1:c.665-20A>G | ||
ENST00000470363.5:n.72A>G | ||
ENST00000487245.5:n.1113A>G | ||
ENST00000495835.1:n.943A>G | ||
NM_002117.5:c.754A>G | NP_002108.4:p.Thr252Ala | |
NM_002117.6:c.754A>G MANE Select | NP_002108.4:p.Thr252Ala |