HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99420714C>T , CM000666.2:g.99420714C>T | GRCh38 |
NC_000004.11:g.100341871C>T , CM000666.1:g.100341871C>T | GRCh37 |
NC_000004.10:g.100560894C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000437033.7:c.644G>A MANE Select | ENSP00000414254.2:p.Gly215Asp | |
ENST00000209665.8:c.680G>A | ENSP00000209665.4:p.Gly227Asp | |
ENST00000437033.6:c.644G>A | ENSP00000414254.2:p.Gly215Asp | |
ENST00000476959.5:c.704G>A | ENSP00000420269.1:p.Gly235Asp | |
ENST00000482593.5:c.473G>A | ENSP00000420613.1:p.Gly158Asp | |
NM_000673.4:c.680G>A | NP_000664.2:p.Gly227Asp | |
NM_001166504.1:c.704G>A | NP_001159976.1:p.Gly235Asp | |
NM_000673.7:c.644G>A MANE Select | NP_000664.3:p.Gly215Asp | |
NM_001166504.2:c.704G>A | NP_001159976.1:p.Gly235Asp |