HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41583857C>G , CM000679.2:g.41583857C>G | GRCh38 |
NC_000017.10:g.39740109C>G , CM000679.1:g.39740109C>G | GRCh37 |
NC_000017.9:g.36993635C>G | NCBI36 |
NG_008624.1:g.8039G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.830G>C MANE Select | ENSP00000167586.6:p.Gly277Ala | |
ENST00000167586.6:c.830G>C | ENSP00000167586.6:p.Gly277Ala | |
ENST00000476662.1:n.280G>C | ||
NM_000526.4:c.830G>C | NP_000517.2:p.Gly277Ala | |
NM_000526.5:c.830G>C MANE Select | NP_000517.3:p.Gly277Ala |