Canonical Allele Identifier: CA393802124

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549299
• gnomAD v4: 15-90088477-T-A
• COSMIC: COSM1375398
• MyVariant Identifiers: chr15:g.90631709T>A (hg19) ; chr15:g.90088477T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088477T>A , CM000677.2:g.90088477T>A	GRCh38
NC_000015.9:g.90631709T>A , CM000677.1:g.90631709T>A	GRCh37
NC_000015.8:g.88432713T>A	NCBI36
NG_023302.1:g.19000A>T , LRG_611:g.19000A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.560A>T MANE Select	ENSP00000331897.4:p.Asp187Val
ENST00000330062.7:c.560A>T	ENSP00000331897.3:p.Asp187Val
ENST00000540499.2:c.404A>T	ENSP00000446147.2:p.Asp135Val
ENST00000559482.5:c.233A>T	ENSP00000453016.1:p.Asp78Val
ENST00000560061.1:c.*185A>T	ENSP00000453254.1:n.*185A>T
NM_001289910.1:c.404A>T , LRG_611t1:c.404A>T	NP_001276839.1:p.Asp135Val
NM_001290114.1:c.170A>T	NP_001277043.1:p.Asp57Val
NM_002168.3:c.560A>T , LRG_611t2:c.560A>T	NP_002159.2:p.Asp187Val
NM_001290114.2:c.170A>T	NP_001277043.1:p.Asp57Val
NM_002168.4:c.560A>T MANE Select	NP_002159.2:p.Asp187Val