HGVS | Genome Assembly |
---|---|
NC_000016.10:g.89919524G= , CM000678.2:g.89919524G= | GRCh38 |
NC_000016.9:g.89985932G= , CM000678.1:g.89985932G= | GRCh37 |
NC_000016.8:g.88513433G= | NCBI36 |
NG_012026.1:g.6646G= | |
NG_027810.1:g.2516G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000555147.2:c.266G= MANE Select | ENSP00000451605.1:p.Gly89= | |
ENST00000639847.1:c.266G= | ENSP00000492011.1:p.Gly89= | |
ENST00000555147.1:c.266G= | ENSP00000451605.1:p.Gly89= | |
ENST00000555427.1:c.266G= | ENSP00000451760.1:p.Gly89= | |
ENST00000556922.1:c.266G= | ENSP00000451560.1:p.Gly89= | |
NM_002386.3:c.266G= | NP_002377.4:p.Gly89= | |
NM_002386.4:c.266G= MANE Select | NP_002377.4:p.Gly89= |