Canonical Allele Identifier: CA2575832585

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549434

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088560G>A , CM000677.2:g.90088560G>A	GRCh38
NC_000015.9:g.90631792G>A , CM000677.1:g.90631792G>A	GRCh37
NC_000015.8:g.88432796G>A	NCBI36
NG_023302.1:g.18917C>T , LRG_611:g.18917C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.534+27C>T MANE Select	ENSP00000331897.4:n.534+27C>T
ENST00000330062.7:c.534+27C>T	ENSP00000331897.3:n.534+27C>T
ENST00000540499.2:c.378+27C>T	ENSP00000446147.2:n.378+27C>T
ENST00000559482.5:c.208-58C>T	ENSP00000453016.1:n.208-58C>T
ENST00000560061.1:c.*159+27C>T	ENSP00000453254.1:n.*159+27C>T
NM_001289910.1:c.378+27C>T , LRG_611t1:c.378+27C>T	NP_001276839.1:n.378+27C>T
NM_001290114.1:c.144+27C>T	NP_001277043.1:n.144+27C>T
NM_002168.3:c.534+27C>T , LRG_611t2:c.534+27C>T	NP_002159.2:n.534+27C>T
NM_001290114.2:c.144+27C>T	NP_001277043.1:n.144+27C>T
NM_002168.4:c.534+27C>T MANE Select	NP_002159.2:n.534+27C>T