Canonical Allele Identifier: CA274623864

Gene: IDH2

Linked Data

• dbSNP Id: rs755016578
• gnomAD v4: 15-90088645-C-T
• COSMIC: COSM966443
• MyVariant Identifiers: chr15:g.90631877C>T (hg19) ; chr15:g.90088645C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088645C>T , CM000677.2:g.90088645C>T	GRCh38
NC_000015.9:g.90631877C>T , CM000677.1:g.90631877C>T	GRCh37
NC_000015.8:g.88432881C>T	NCBI36
NG_023302.1:g.18832G>A , LRG_611:g.18832G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.476G>A MANE Select	ENSP00000331897.4:p.Arg159His
ENST00000330062.7:c.476G>A	ENSP00000331897.3:p.Arg159His
ENST00000540499.2:c.320G>A	ENSP00000446147.2:p.Arg107His
ENST00000559482.5:c.208-143G>A	ENSP00000453016.1:n.208-143G>A
ENST00000560061.1:c.*101G>A	ENSP00000453254.1:n.*101G>A
NM_001289910.1:c.320G>A , LRG_611t1:c.320G>A	NP_001276839.1:p.Arg107His
NM_001290114.1:c.86G>A	NP_001277043.1:p.Arg29His
NM_002168.3:c.476G>A , LRG_611t2:c.476G>A	NP_002159.2:p.Arg159His
NM_001290114.2:c.86G>A	NP_001277043.1:p.Arg29His
NM_002168.4:c.476G>A MANE Select	NP_002159.2:p.Arg159His