Canonical Allele Identifier: CA656779172

Gene: IDH2

Linked Data

• dbSNP Id: rs1900935932
• COSMIC: COSN19229828

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088523C>T , CM000677.2:g.90088523C>T	GRCh38
NC_000015.9:g.90631755C>T , CM000677.1:g.90631755C>T	GRCh37
NC_000015.8:g.88432759C>T	NCBI36
NG_023302.1:g.18954G>A , LRG_611:g.18954G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.535-21G>A MANE Select	ENSP00000331897.4:n.535-21G>A
ENST00000330062.7:c.535-21G>A	ENSP00000331897.3:n.535-21G>A
ENST00000540499.2:c.379-21G>A	ENSP00000446147.2:n.379-21G>A
ENST00000559482.5:c.208-21G>A	ENSP00000453016.1:n.208-21G>A
ENST00000560061.1:c.*160-21G>A	ENSP00000453254.1:n.*160-21G>A
NM_001289910.1:c.379-21G>A , LRG_611t1:c.379-21G>A	NP_001276839.1:n.379-21G>A
NM_001290114.1:c.145-21G>A	NP_001277043.1:n.145-21G>A
NM_002168.3:c.535-21G>A , LRG_611t2:c.535-21G>A	NP_002159.2:n.535-21G>A
NM_001290114.2:c.145-21G>A	NP_001277043.1:n.145-21G>A
NM_002168.4:c.535-21G>A MANE Select	NP_002159.2:n.535-21G>A