Canonical Allele Identifier: CA2194954414

Gene: IDH2

Linked Data

• dbSNP Id: rs1366926870

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088546G>T , CM000677.2:g.90088546G>T	GRCh38
NC_000015.9:g.90631778G>T , CM000677.1:g.90631778G>T	GRCh37
NC_000015.8:g.88432782G>T	NCBI36
NG_023302.1:g.18931C>A , LRG_611:g.18931C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.534+41C>A MANE Select	ENSP00000331897.4:n.534+41C>A
ENST00000330062.7:c.534+41C>A	ENSP00000331897.3:n.534+41C>A
ENST00000540499.2:c.378+41C>A	ENSP00000446147.2:n.378+41C>A
ENST00000559482.5:c.208-44C>A	ENSP00000453016.1:n.208-44C>A
ENST00000560061.1:c.*159+41C>A	ENSP00000453254.1:n.*159+41C>A
NM_001289910.1:c.378+41C>A , LRG_611t1:c.378+41C>A	NP_001276839.1:n.378+41C>A
NM_001290114.1:c.144+41C>A	NP_001277043.1:n.144+41C>A
NM_002168.3:c.534+41C>A , LRG_611t2:c.534+41C>A	NP_002159.2:n.534+41C>A
NM_001290114.2:c.144+41C>A	NP_001277043.1:n.144+41C>A
NM_002168.4:c.534+41C>A MANE Select	NP_002159.2:n.534+41C>A