HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99420784C= , CM000666.2:g.99420784C= | GRCh38 |
NC_000004.11:g.100341941C= , CM000666.1:g.100341941C= | GRCh37 |
NC_000004.10:g.100560964C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437033.7:c.574G= MANE Select | ENSP00000414254.2:p.Gly192= | |
ENST00000209665.8:c.610G= | ENSP00000209665.4:p.Gly204= | |
ENST00000437033.6:c.574G= | ENSP00000414254.2:p.Gly192= | |
ENST00000476959.5:c.634G= | ENSP00000420269.1:p.Gly212= | |
ENST00000482593.5:c.403G= | ENSP00000420613.1:p.Gly135= | |
NM_000673.4:c.610G= | NP_000664.2:p.Gly204= | |
NM_001166504.1:c.634G= | NP_001159976.1:p.Gly212= | |
NM_000673.7:c.574G= MANE Select | NP_000664.3:p.Gly192= | |
NM_001166504.2:c.634G= | NP_001159976.1:p.Gly212= |