Canonical Allele Identifier: CA393802107

Gene: IDH2

Linked Data

• dbSNP Id: rs1900933568
• gnomAD v3: 15-90088466-T-G
• gnomAD v4: 15-90088466-T-G
• MyVariant Identifiers: chr15:g.90631698T>G (hg19) ; chr15:g.90088466T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088466T>G , CM000677.2:g.90088466T>G	GRCh38
NC_000015.9:g.90631698T>G , CM000677.1:g.90631698T>G	GRCh37
NC_000015.8:g.88432702T>G	NCBI36
NG_023302.1:g.19011A>C , LRG_611:g.19011A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.571A>C MANE Select	ENSP00000331897.4:p.Thr191Pro
ENST00000330062.7:c.571A>C	ENSP00000331897.3:p.Thr191Pro
ENST00000540499.2:c.415A>C	ENSP00000446147.2:p.Thr139Pro
ENST00000559482.5:c.244A>C	ENSP00000453016.1:p.Thr82Pro
ENST00000560061.1:c.*196A>C	ENSP00000453254.1:n.*196A>C
NM_001289910.1:c.415A>C , LRG_611t1:c.415A>C	NP_001276839.1:p.Thr139Pro
NM_001290114.1:c.181A>C	NP_001277043.1:p.Thr61Pro
NM_002168.3:c.571A>C , LRG_611t2:c.571A>C	NP_002159.2:p.Thr191Pro
NM_001290114.2:c.181A>C	NP_001277043.1:p.Thr61Pro
NM_002168.4:c.571A>C MANE Select	NP_002159.2:p.Thr191Pro