Canonical Allele Identifier: CA619547903

Gene: IDH2

Linked Data

• dbSNP Id: rs1330843926
• gnomAD v2: 15-90632064-C-CG
• gnomAD v3: 15-90088832-C-CG
• gnomAD v4: 15-90088832-C-CG
• MyVariant Identifiers: chr15:g.90632064_90632065insG (hg19) ; chr15:g.90088832_90088833insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088837dup , CM000677.2:g.90088837dup	GRCh38
NC_000015.9:g.90632069dup , CM000677.1:g.90632069dup	GRCh37
NC_000015.8:g.88433073dup	NCBI36
NG_023302.1:g.18644dup , LRG_611:g.18644dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.374-86dup MANE Select	ENSP00000331897.4:n.374-86dup
ENST00000330062.7:c.374-86dup	ENSP00000331897.3:n.374-86dup
ENST00000540499.2:c.218-86dup	ENSP00000446147.2:n.218-86dup
ENST00000559482.5:c.208-331dup	ENSP00000453016.1:n.208-331dup
ENST00000560061.1:c.116-86dup	ENSP00000453254.1:n.116-86dup
NM_001289910.1:c.218-86dup , LRG_611t1:c.218-86dup	NP_001276839.1:n.218-86dup
NM_001290114.1:c.-17-86dup	NP_001277043.1:n.-17-86dup
NM_002168.3:c.374-86dup , LRG_611t2:c.374-86dup	NP_002159.2:n.374-86dup
NM_001290114.2:c.-17-86dup	NP_001277043.1:n.-17-86dup
NM_002168.4:c.374-86dup MANE Select	NP_002159.2:n.374-86dup