Canonical Allele Identifier: CA274623691

Gene: IDH2

Linked Data

• dbSNP Id: rs868324434
• COSMIC: COSM2139737
• MyVariant Identifiers: chr15:g.90631700C>T (hg19) ; chr15:g.90088468C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088468C>T , CM000677.2:g.90088468C>T	GRCh38
NC_000015.9:g.90631700C>T , CM000677.1:g.90631700C>T	GRCh37
NC_000015.8:g.88432704C>T	NCBI36
NG_023302.1:g.19009G>A , LRG_611:g.19009G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.569G>A MANE Select	ENSP00000331897.4:p.Gly190Asp
ENST00000330062.7:c.569G>A	ENSP00000331897.3:p.Gly190Asp
ENST00000540499.2:c.413G>A	ENSP00000446147.2:p.Gly138Asp
ENST00000559482.5:c.242G>A	ENSP00000453016.1:p.Gly81Asp
ENST00000560061.1:c.*194G>A	ENSP00000453254.1:n.*194G>A
NM_001289910.1:c.413G>A , LRG_611t1:c.413G>A	NP_001276839.1:p.Gly138Asp
NM_001290114.1:c.179G>A	NP_001277043.1:p.Gly60Asp
NM_002168.3:c.569G>A , LRG_611t2:c.569G>A	NP_002159.2:p.Gly190Asp
NM_001290114.2:c.179G>A	NP_001277043.1:p.Gly60Asp
NM_002168.4:c.569G>A MANE Select	NP_002159.2:p.Gly190Asp