Canonical Allele Identifier: CA7733232
Community Standard Title: NM_002168.4(IDH2):c.266G>A (p.Arg89His)
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90090586C>T , CM000677.2:g.90090586C>T GRCh38
NC_000015.9:g.90633818C>T , CM000677.1:g.90633818C>T GRCh37
NC_000015.8:g.88434822C>T NCBI36
NG_023302.1:g.16891G>A , LRG_611:g.16891G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002168.4:c.266G>A MANE Select NP_002159.2:p.Arg89His
ENST00000330062.8:c.266G>A MANE Select ENSP00000331897.4:p.Arg89His
NM_001289910.1:c.110G>A , LRG_611t1:c.110G>A NP_001276839.1:p.Arg37His
NM_001290114.1:c.-17-1839G>A NP_001277043.1:n.-17-1839G>A
NM_001290114.2:c.-17-1839G>A NP_001277043.1:n.-17-1839G>A
NM_002168.3:c.266G>A , LRG_611t2:c.266G>A NP_002159.2:p.Arg89His
ENST00000330062.7:c.266G>A ENSP00000331897.3:p.Arg89His
ENST00000540499.2:c.110G>A ENSP00000446147.2:p.Arg37His
ENST00000559482.5:c.207+967G>A ENSP00000453016.1:n.207+967G>A
ENST00000560061.1:c.116-1839G>A ENSP00000453254.1:n.116-1839G>A