Canonical Allele Identifier: CA2194954380
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088486A= , CM000677.2:g.90088486A= GRCh38
NC_000015.9:g.90631718A= , CM000677.1:g.90631718A= GRCh37
NC_000015.8:g.88432722A= NCBI36
NG_023302.1:g.18991T= , LRG_611:g.18991T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.551T= MANE Select ENSP00000331897.4:p.Phe184=
ENST00000330062.7:c.551T= ENSP00000331897.3:p.Phe184=
ENST00000540499.2:c.395T= ENSP00000446147.2:p.Phe132=
ENST00000559482.5:c.224T= ENSP00000453016.1:p.Phe75=
ENST00000560061.1:c.*176T= ENSP00000453254.1:n.*176T=
NM_001289910.1:c.395T= , LRG_611t1:c.395T= NP_001276839.1:p.Phe132=
NM_001290114.1:c.161T= NP_001277043.1:p.Phe54=
NM_002168.3:c.551T= , LRG_611t2:c.551T= NP_002159.2:p.Phe184=
NM_001290114.2:c.161T= NP_001277043.1:p.Phe54=
NM_002168.4:c.551T= MANE Select NP_002159.2:p.Phe184=