Canonical Allele Identifier: CA393802035
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs2151549241

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088435C>A , CM000677.2:g.90088435C>A GRCh38
NC_000015.9:g.90631667C>A , CM000677.1:g.90631667C>A GRCh37
NC_000015.8:g.88432671C>A NCBI36
NG_023302.1:g.19042G>T , LRG_611:g.19042G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.602G>T MANE Select ENSP00000331897.4:p.Gly201Val
ENST00000330062.7:c.602G>T ENSP00000331897.3:p.Gly201Val
ENST00000540499.2:c.446G>T ENSP00000446147.2:p.Gly149Val
ENST00000559482.5:c.275G>T ENSP00000453016.1:p.Gly92Val
ENST00000560061.1:c.*227G>T ENSP00000453254.1:n.*227G>T
NM_001289910.1:c.446G>T , LRG_611t1:c.446G>T NP_001276839.1:p.Gly149Val
NM_001290114.1:c.212G>T NP_001277043.1:p.Gly71Val
NM_002168.3:c.602G>T , LRG_611t2:c.602G>T NP_002159.2:p.Gly201Val
NM_001290114.2:c.212G>T NP_001277043.1:p.Gly71Val
NM_002168.4:c.602G>T MANE Select NP_002159.2:p.Gly201Val