HGVS | Genome Assembly |
---|---|
NC_000011.10:g.124872918G= , CM000673.2:g.124872918G= | GRCh38 |
NC_000011.9:g.124742814G= , CM000673.1:g.124742814G= | GRCh37 |
NC_000011.8:g.124248024G= | NCBI36 |
NG_016214.1:g.12510G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000397801.6:c.1365G= MANE Select | ENSP00000380903.1:p.Gln455= | |
ENST00000397801.5:c.1365G= | ENSP00000380903.1:p.Gln455= | |
ENST00000538940.5:c.1299G= | ENSP00000441797.1:p.Gln433= | |
NM_022370.3:c.1365G= | NP_071765.2:p.Gln455= | |
XM_011542953.1:c.2337G= | XP_011541255.1:p.Gln779= | |
XM_017018122.1:c.1299G= | XP_016873611.1:p.Gln433= | |
NM_022370.4:c.1365G= MANE Select | NP_071765.2:p.Gln455= |