HGVS | Genome Assembly |
---|---|
NC_000015.10:g.84840208A>C , CM000677.2:g.84840208A>C | GRCh38 |
NC_000015.9:g.85383439A>C , CM000677.1:g.85383439A>C | GRCh37 |
NC_000015.8:g.83184443A>C | NCBI36 |
NG_054748.1:g.28578A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258888.6:c.929A>C MANE Select | ENSP00000258888.6:p.Glu310Ala | |
ENST00000258888.5:c.1535A>C | ENSP00000258888.5:p.Glu512Ala | |
NM_020778.4:c.1535A>C | NP_065829.3:p.Glu512Ala | |
NM_020778.5:c.929A>C MANE Select | NP_065829.4:p.Glu310Ala |