Canonical Allele Identifier: CA2731558940

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549457

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088569C>A , CM000677.2:g.90088569C>A	GRCh38
NC_000015.9:g.90631801C>A , CM000677.1:g.90631801C>A	GRCh37
NC_000015.8:g.88432805C>A	NCBI36
NG_023302.1:g.18908G>T , LRG_611:g.18908G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.534+18G>T MANE Select	ENSP00000331897.4:n.534+18G>T
ENST00000330062.7:c.534+18G>T	ENSP00000331897.3:n.534+18G>T
ENST00000540499.2:c.378+18G>T	ENSP00000446147.2:n.378+18G>T
ENST00000559482.5:c.208-67G>T	ENSP00000453016.1:n.208-67G>T
ENST00000560061.1:c.*159+18G>T	ENSP00000453254.1:n.*159+18G>T
NM_001289910.1:c.378+18G>T , LRG_611t1:c.378+18G>T	NP_001276839.1:n.378+18G>T
NM_001290114.1:c.144+18G>T	NP_001277043.1:n.144+18G>T
NM_002168.3:c.534+18G>T , LRG_611t2:c.534+18G>T	NP_002159.2:n.534+18G>T
NM_001290114.2:c.144+18G>T	NP_001277043.1:n.144+18G>T
NM_002168.4:c.534+18G>T MANE Select	NP_002159.2:n.534+18G>T