Canonical Allele Identifier: CA2194954358
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088446G= , CM000677.2:g.90088446G= GRCh38
NC_000015.9:g.90631678G= , CM000677.1:g.90631678G= GRCh37
NC_000015.8:g.88432682G= NCBI36
NG_023302.1:g.19031C= , LRG_611:g.19031C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.591C= MANE Select ENSP00000331897.4:p.Thr197=
ENST00000330062.7:c.591C= ENSP00000331897.3:p.Thr197=
ENST00000540499.2:c.435C= ENSP00000446147.2:p.Thr145=
ENST00000559482.5:c.264C= ENSP00000453016.1:p.Thr88=
ENST00000560061.1:c.*216C= ENSP00000453254.1:n.*216C=
NM_001289910.1:c.435C= , LRG_611t1:c.435C= NP_001276839.1:p.Thr145=
NM_001290114.1:c.201C= NP_001277043.1:p.Thr67=
NM_002168.3:c.591C= , LRG_611t2:c.591C= NP_002159.2:p.Thr197=
NM_001290114.2:c.201C= NP_001277043.1:p.Thr67=
NM_002168.4:c.591C= MANE Select NP_002159.2:p.Thr197=