HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23375738A>G , CM000676.2:g.23375738A>G | GRCh38 |
NC_000014.8:g.23844947A>G , CM000676.1:g.23844947A>G | GRCh37 |
NC_000014.7:g.22914787A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000397242.3:c.344A>G MANE Select | ENSP00000380417.2:p.Glu115Gly | |
ENST00000329715.2:c.392A>G | ENSP00000328111.2:p.Glu131Gly | |
ENST00000397242.2:c.344A>G | ENSP00000380417.2:p.Glu115Gly | |
NM_022789.3:c.392A>G | NP_073626.1:p.Glu131Gly | |
NM_172314.1:c.344A>G | NP_758525.1:p.Glu115Gly |