HGVS | Genome Assembly |
---|---|
NC_000014.9:g.93218656G>A , CM000676.2:g.93218656G>A | GRCh38 |
NC_000014.8:g.93685002G>A , CM000676.1:g.93685002G>A | GRCh37 |
NC_000014.7:g.92754755G>A | NCBI36 |
NG_051089.1:g.16601G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000013070.11:c.731G>A MANE Select | ENSP00000013070.6:p.Gly244Glu | |
ENST00000013070.10:c.731G>A | ENSP00000013070.6:p.Gly244Glu | |
ENST00000416753.5:c.503G>A | ENSP00000391706.2:p.Gly168Glu | |
ENST00000553674.1:c.*432G>A | ENSP00000450470.1:n.*432G>A | |
ENST00000553857.5:c.378+3375G>A | ||
ENST00000556871.5:c.440G>A | ENSP00000451022.1:p.Gly147Glu | |
NM_175748.3:c.731G>A | NP_786924.2:p.Gly244Glu | |
NR_038150.1:n.833G>A | ||
NM_175748.4:c.731G>A MANE Select | NP_786924.2:p.Gly244Glu | |
NR_038150.2:n.633G>A |