Canonical Allele Identifier: CA2731277491

Gene: IDH2

Linked Data

• dbSNP Id: rs1415271670

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088557T>A , CM000677.2:g.90088557T>A	GRCh38
NC_000015.9:g.90631789T>A , CM000677.1:g.90631789T>A	GRCh37
NC_000015.8:g.88432793T>A	NCBI36
NG_023302.1:g.18920A>T , LRG_611:g.18920A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.534+30A>T MANE Select	ENSP00000331897.4:n.534+30A>T
ENST00000330062.7:c.534+30A>T	ENSP00000331897.3:n.534+30A>T
ENST00000540499.2:c.378+30A>T	ENSP00000446147.2:n.378+30A>T
ENST00000559482.5:c.208-55A>T	ENSP00000453016.1:n.208-55A>T
ENST00000560061.1:c.*159+30A>T	ENSP00000453254.1:n.*159+30A>T
NM_001289910.1:c.378+30A>T , LRG_611t1:c.378+30A>T	NP_001276839.1:n.378+30A>T
NM_001290114.1:c.144+30A>T	NP_001277043.1:n.144+30A>T
NM_002168.3:c.534+30A>T , LRG_611t2:c.534+30A>T	NP_002159.2:n.534+30A>T
NM_001290114.2:c.144+30A>T	NP_001277043.1:n.144+30A>T
NM_002168.4:c.534+30A>T MANE Select	NP_002159.2:n.534+30A>T