HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94047066C>T , CM000663.2:g.94047066C>T | GRCh38 |
NC_000001.10:g.94512622C>T , CM000663.1:g.94512622C>T | GRCh37 |
NC_000001.9:g.94285210C>T | NCBI36 |
NG_009073.1:g.79084G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.2771G>A MANE Select | ENSP00000359245.3:p.Gly924Glu | |
ENST00000649773.1:c.2549G>A | ENSP00000496882.1:p.Gly850Glu | |
ENST00000370225.3:c.2771G>A | ENSP00000359245.3:p.Gly924Glu | |
ENST00000536513.5:c.-64-6977G>A | ENSP00000439707.2:n.-64-6977G>A | |
NM_000350.2:c.2771G>A | NP_000341.2:p.Gly924Glu | |
NM_000350.3:c.2771G>A MANE Select | NP_000341.2:p.Gly924Glu |