HGVS | Genome Assembly |
---|---|
NC_000015.10:g.84840244A>C , CM000677.2:g.84840244A>C | GRCh38 |
NC_000015.9:g.85383475A>C , CM000677.1:g.85383475A>C | GRCh37 |
NC_000015.8:g.83184479A>C | NCBI36 |
NG_054748.1:g.28614A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258888.6:c.965A>C MANE Select | ENSP00000258888.6:p.Glu322Ala | |
ENST00000258888.5:c.1571A>C | ENSP00000258888.5:p.Glu524Ala | |
NM_020778.4:c.1571A>C | NP_065829.3:p.Glu524Ala | |
NM_020778.5:c.965A>C MANE Select | NP_065829.4:p.Glu322Ala |