HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52033592C= , CM000666.2:g.52033592C= | GRCh38 |
NC_000004.11:g.52899758C= , CM000666.1:g.52899758C= | GRCh37 |
NC_000004.10:g.52594515C= | NCBI36 |
NG_008891.1:g.9728G= , LRG_204:g.9728G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.82G= MANE Select | ENSP00000370839.6:p.Glu28= | |
ENST00000381431.9:c.82G= | ENSP00000370839.5:p.Glu28= | |
ENST00000506357.5:c.68G= | ||
ENST00000514133.1:c.49G= | ENSP00000425818.1:p.Glu17= | |
NM_000232.4:c.82G= , LRG_204t1:c.82G= | NP_000223.1:p.Glu28= | |
XM_011534403.1:c.34-3729G= | XP_011532705.1:n.34-3729G= | |
NM_000232.5:c.82G= MANE Select | NP_000223.1:p.Glu28= |