Canonical Allele Identifier: CA393802222
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs1900938886

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088598G>A , CM000677.2:g.90088598G>A GRCh38
NC_000015.9:g.90631830G>A , CM000677.1:g.90631830G>A GRCh37
NC_000015.8:g.88432834G>A NCBI36
NG_023302.1:g.18879C>T , LRG_611:g.18879C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.523C>T MANE Select ENSP00000331897.4:p.His175Tyr
ENST00000330062.7:c.523C>T ENSP00000331897.3:p.His175Tyr
ENST00000540499.2:c.367C>T ENSP00000446147.2:p.His123Tyr
ENST00000559482.5:c.208-96C>T ENSP00000453016.1:n.208-96C>T
ENST00000560061.1:c.*148C>T ENSP00000453254.1:n.*148C>T
NM_001289910.1:c.367C>T , LRG_611t1:c.367C>T NP_001276839.1:p.His123Tyr
NM_001290114.1:c.133C>T NP_001277043.1:p.His45Tyr
NM_002168.3:c.523C>T , LRG_611t2:c.523C>T NP_002159.2:p.His175Tyr
NM_001290114.2:c.133C>T NP_001277043.1:p.His45Tyr
NM_002168.4:c.523C>T MANE Select NP_002159.2:p.His175Tyr