Canonical Allele Identifier: CA393802239

Gene: IDH2

Linked Data

• dbSNP Id: rs121913503
• COSMIC: COSM1636997
• MyVariant Identifiers: chr15:g.90631838C>G (hg19) ; chr15:g.90088606C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088606C>G , CM000677.2:g.90088606C>G	GRCh38
NC_000015.9:g.90631838C>G , CM000677.1:g.90631838C>G	GRCh37
NC_000015.8:g.88432842C>G	NCBI36
NG_023302.1:g.18871G>C , LRG_611:g.18871G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000330062.8:c.515G>C MANE Select	ENSP00000331897.4:p.Arg172Thr
ENST00000330062.7:c.515G>C	ENSP00000331897.3:p.Arg172Thr
ENST00000540499.2:c.359G>C	ENSP00000446147.2:p.Arg120Thr
ENST00000559482.5:c.208-104G>C	ENSP00000453016.1:n.208-104G>C
ENST00000560061.1:c.*140G>C	ENSP00000453254.1:n.*140G>C
NM_001289910.1:c.359G>C , LRG_611t1:c.359G>C	NP_001276839.1:p.Arg120Thr
NM_001290114.1:c.125G>C	NP_001277043.1:p.Arg42Thr
NM_002168.3:c.515G>C , LRG_611t2:c.515G>C	NP_002159.2:p.Arg172Thr
NM_001290114.2:c.125G>C	NP_001277043.1:p.Arg42Thr
NM_002168.4:c.515G>C MANE Select	NP_002159.2:p.Arg172Thr