HGVS | Genome Assembly |
---|---|
NC_000016.10:g.89919927G= , CM000678.2:g.89919927G= | GRCh38 |
NC_000016.9:g.89986335G= , CM000678.1:g.89986335G= | GRCh37 |
NC_000016.8:g.88513836G= | NCBI36 |
NG_012026.1:g.7049G= | |
NG_027810.1:g.2919G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555147.2:c.669G= MANE Select | ENSP00000451605.1:p.Arg223= | |
ENST00000639847.1:c.669G= | ENSP00000492011.1:p.Arg223= | |
ENST00000555147.1:c.669G= | ENSP00000451605.1:p.Arg223= | |
ENST00000555427.1:c.669G= | ENSP00000451760.1:p.Arg223= | |
ENST00000556922.1:c.669G= | ENSP00000451560.1:p.Arg223= | |
NM_002386.3:c.669G= | NP_002377.4:p.Arg223= | |
NM_002386.4:c.669G= MANE Select | NP_002377.4:p.Arg223= |