Canonical Allele Identifier: CA619859354

Gene: IDH2

Linked Data

• dbSNP Id: rs1274155953
• gnomAD v2: 15-90631748-A-AG
• gnomAD v4: 15-90088516-A-AG
• MyVariant Identifiers: chr15:g.90631748_90631749insG (hg19) ; chr15:g.90088516_90088517insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088518dup , CM000677.2:g.90088518dup	GRCh38
NC_000015.9:g.90631750dup , CM000677.1:g.90631750dup	GRCh37
NC_000015.8:g.88432754dup	NCBI36
NG_023302.1:g.18960dup , LRG_611:g.18960dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.535-15dup MANE Select	ENSP00000331897.4:n.535-15dup
ENST00000330062.7:c.535-15dup	ENSP00000331897.3:n.535-15dup
ENST00000540499.2:c.379-15dup	ENSP00000446147.2:n.379-15dup
ENST00000559482.5:c.208-15dup	ENSP00000453016.1:n.208-15dup
ENST00000560061.1:c.*160-15dup	ENSP00000453254.1:n.*160-15dup
NM_001289910.1:c.379-15dup , LRG_611t1:c.379-15dup	NP_001276839.1:n.379-15dup
NM_001290114.1:c.145-15dup	NP_001277043.1:n.145-15dup
NM_002168.3:c.535-15dup , LRG_611t2:c.535-15dup	NP_002159.2:n.535-15dup
NM_001290114.2:c.145-15dup	NP_001277043.1:n.145-15dup
NM_002168.4:c.535-15dup MANE Select	NP_002159.2:n.535-15dup