Canonical Allele Identifier: CA393802293

Gene: IDH2

Linked Data

• dbSNP Id: rs1435266782
• gnomAD v2: 15-90631865-C-T
• gnomAD v4: 15-90088633-C-T
• COSMIC: COSM4774901
• MyVariant Identifiers: chr15:g.90631865C>T (hg19) ; chr15:g.90088633C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088633C>T , CM000677.2:g.90088633C>T	GRCh38
NC_000015.9:g.90631865C>T , CM000677.1:g.90631865C>T	GRCh37
NC_000015.8:g.88432869C>T	NCBI36
NG_023302.1:g.18844G>A , LRG_611:g.18844G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.488G>A MANE Select	ENSP00000331897.4:p.Gly163Asp
ENST00000330062.7:c.488G>A	ENSP00000331897.3:p.Gly163Asp
ENST00000540499.2:c.332G>A	ENSP00000446147.2:p.Gly111Asp
ENST00000559482.5:c.208-131G>A	ENSP00000453016.1:n.208-131G>A
ENST00000560061.1:c.*113G>A	ENSP00000453254.1:n.*113G>A
NM_001289910.1:c.332G>A , LRG_611t1:c.332G>A	NP_001276839.1:p.Gly111Asp
NM_001290114.1:c.98G>A	NP_001277043.1:p.Gly33Asp
NM_002168.3:c.488G>A , LRG_611t2:c.488G>A	NP_002159.2:p.Gly163Asp
NM_001290114.2:c.98G>A	NP_001277043.1:p.Gly33Asp
NM_002168.4:c.488G>A MANE Select	NP_002159.2:p.Gly163Asp