Canonical Allele Identifier: CA7733165

Gene: IDH2

Linked Data

• dbSNP Id: rs770371757
• ExAC: 15:90631802 T / A
• gnomAD v2: 15-90631802-T-A
• gnomAD v4: 15-90088570-T-A
• MyVariant Identifiers: chr15:g.90631802T>A (hg19) ; chr15:g.90088570T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088570T>A , CM000677.2:g.90088570T>A	GRCh38
NC_000015.9:g.90631802T>A , CM000677.1:g.90631802T>A	GRCh37
NC_000015.8:g.88432806T>A	NCBI36
NG_023302.1:g.18907A>T , LRG_611:g.18907A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.534+17A>T MANE Select	ENSP00000331897.4:n.534+17A>T
ENST00000330062.7:c.534+17A>T	ENSP00000331897.3:n.534+17A>T
ENST00000540499.2:c.378+17A>T	ENSP00000446147.2:n.378+17A>T
ENST00000559482.5:c.208-68A>T	ENSP00000453016.1:n.208-68A>T
ENST00000560061.1:c.*159+17A>T	ENSP00000453254.1:n.*159+17A>T
NM_001289910.1:c.378+17A>T , LRG_611t1:c.378+17A>T	NP_001276839.1:n.378+17A>T
NM_001290114.1:c.144+17A>T	NP_001277043.1:n.144+17A>T
NM_002168.3:c.534+17A>T , LRG_611t2:c.534+17A>T	NP_002159.2:n.534+17A>T
NM_001290114.2:c.144+17A>T	NP_001277043.1:n.144+17A>T
NM_002168.4:c.534+17A>T MANE Select	NP_002159.2:n.534+17A>T