Canonical Allele Identifier: CA7733126

Gene: IDH2

Linked Data

• ClinVar Variation Id: 1336977
• ClinVar RCV Id: RCV001819463
• dbSNP Id: rs761404149
• ExAC: 15:90631647 C / T
• gnomAD v2: 15-90631647-C-T
• gnomAD v4: 15-90088415-C-T
• MyVariant Identifiers: chr15:g.90631647C>T (hg19) ; chr15:g.90088415C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088415C>T , CM000677.2:g.90088415C>T	GRCh38
NC_000015.9:g.90631647C>T , CM000677.1:g.90631647C>T	GRCh37
NC_000015.8:g.88432651C>T	NCBI36
NG_023302.1:g.19062G>A , LRG_611:g.19062G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.622G>A MANE Select	ENSP00000331897.4:p.Glu208Lys
ENST00000330062.7:c.622G>A	ENSP00000331897.3:p.Glu208Lys
ENST00000540499.2:c.466G>A	ENSP00000446147.2:p.Glu156Lys
ENST00000559482.5:c.295G>A	ENSP00000453016.1:p.Glu99Lys
ENST00000560061.1:c.*247G>A	ENSP00000453254.1:n.*247G>A
NM_001289910.1:c.466G>A , LRG_611t1:c.466G>A	NP_001276839.1:p.Glu156Lys
NM_001290114.1:c.232G>A	NP_001277043.1:p.Glu78Lys
NM_002168.3:c.622G>A , LRG_611t2:c.622G>A	NP_002159.2:p.Glu208Lys
NM_001290114.2:c.232G>A	NP_001277043.1:p.Glu78Lys
NM_002168.4:c.622G>A MANE Select	NP_002159.2:p.Glu208Lys