Canonical Allele Identifier: CA7733162

Gene: IDH2

Linked Data

• dbSNP Id: rs777479451
• ExAC: 15:90631797 T / A
• gnomAD v2: 15-90631797-T-A
• gnomAD v3: 15-90088565-T-A
• gnomAD v4: 15-90088565-T-A
• MyVariant Identifiers: chr15:g.90631797T>A (hg19) ; chr15:g.90088565T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088565T>A , CM000677.2:g.90088565T>A	GRCh38
NC_000015.9:g.90631797T>A , CM000677.1:g.90631797T>A	GRCh37
NC_000015.8:g.88432801T>A	NCBI36
NG_023302.1:g.18912A>T , LRG_611:g.18912A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.534+22A>T MANE Select	ENSP00000331897.4:n.534+22A>T
ENST00000330062.7:c.534+22A>T	ENSP00000331897.3:n.534+22A>T
ENST00000540499.2:c.378+22A>T	ENSP00000446147.2:n.378+22A>T
ENST00000559482.5:c.208-63A>T	ENSP00000453016.1:n.208-63A>T
ENST00000560061.1:c.*159+22A>T	ENSP00000453254.1:n.*159+22A>T
NM_001289910.1:c.378+22A>T , LRG_611t1:c.378+22A>T	NP_001276839.1:n.378+22A>T
NM_001290114.1:c.144+22A>T	NP_001277043.1:n.144+22A>T
NM_002168.3:c.534+22A>T , LRG_611t2:c.534+22A>T	NP_002159.2:n.534+22A>T
NM_001290114.2:c.144+22A>T	NP_001277043.1:n.144+22A>T
NM_002168.4:c.534+22A>T MANE Select	NP_002159.2:n.534+22A>T