Canonical Allele Identifier: CA393802122

Gene: IDH2

Linked Data

• dbSNP Id: rs1160367297
• MyVariant Identifiers: chr15:g.90631708G>C (hg19) ; chr15:g.90088476G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088476G>C , CM000677.2:g.90088476G>C	GRCh38
NC_000015.9:g.90631708G>C , CM000677.1:g.90631708G>C	GRCh37
NC_000015.8:g.88432712G>C	NCBI36
NG_023302.1:g.19001C>G , LRG_611:g.19001C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.561C>G MANE Select	ENSP00000331897.4:p.Asp187Glu
ENST00000330062.7:c.561C>G	ENSP00000331897.3:p.Asp187Glu
ENST00000540499.2:c.405C>G	ENSP00000446147.2:p.Asp135Glu
ENST00000559482.5:c.234C>G	ENSP00000453016.1:p.Asp78Glu
ENST00000560061.1:c.*186C>G	ENSP00000453254.1:n.*186C>G
NM_001289910.1:c.405C>G , LRG_611t1:c.405C>G	NP_001276839.1:p.Asp135Glu
NM_001290114.1:c.171C>G	NP_001277043.1:p.Asp57Glu
NM_002168.3:c.561C>G , LRG_611t2:c.561C>G	NP_002159.2:p.Asp187Glu
NM_001290114.2:c.171C>G	NP_001277043.1:p.Asp57Glu
NM_002168.4:c.561C>G MANE Select	NP_002159.2:p.Asp187Glu