Canonical Allele Identifier: CA7733145

Gene: IDH2

Linked Data

• dbSNP Id: rs772650285
• ExAC: 15:90631726 G / C
• gnomAD v2: 15-90631726-G-C
• gnomAD v4: 15-90088494-G-C
• MyVariant Identifiers: chr15:g.90631726G>C (hg19) ; chr15:g.90088494G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088494G>C , CM000677.2:g.90088494G>C	GRCh38
NC_000015.9:g.90631726G>C , CM000677.1:g.90631726G>C	GRCh37
NC_000015.8:g.88432730G>C	NCBI36
NG_023302.1:g.18983C>G , LRG_611:g.18983C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.543C>G MANE Select	ENSP00000331897.4:p.Ala181=
ENST00000330062.7:c.543C>G	ENSP00000331897.3:p.Ala181=
ENST00000540499.2:c.387C>G	ENSP00000446147.2:p.Ala129=
ENST00000559482.5:c.216C>G	ENSP00000453016.1:p.Ala72=
ENST00000560061.1:c.*168C>G	ENSP00000453254.1:n.*168C>G
NM_001289910.1:c.387C>G , LRG_611t1:c.387C>G	NP_001276839.1:p.Ala129=
NM_001290114.1:c.153C>G	NP_001277043.1:p.Ala51=
NM_002168.3:c.543C>G , LRG_611t2:c.543C>G	NP_002159.2:p.Ala181=
NM_001290114.2:c.153C>G	NP_001277043.1:p.Ala51=
NM_002168.4:c.543C>G MANE Select	NP_002159.2:p.Ala181=