Canonical Allele Identifier: CA393802035

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549241
• MyVariant Identifiers: chr15:g.90631667C>A (hg19) ; chr15:g.90088435C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088435C>A , CM000677.2:g.90088435C>A	GRCh38
NC_000015.9:g.90631667C>A , CM000677.1:g.90631667C>A	GRCh37
NC_000015.8:g.88432671C>A	NCBI36
NG_023302.1:g.19042G>T , LRG_611:g.19042G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.602G>T MANE Select	ENSP00000331897.4:p.Gly201Val
ENST00000330062.7:c.602G>T	ENSP00000331897.3:p.Gly201Val
ENST00000540499.2:c.446G>T	ENSP00000446147.2:p.Gly149Val
ENST00000559482.5:c.275G>T	ENSP00000453016.1:p.Gly92Val
ENST00000560061.1:c.*227G>T	ENSP00000453254.1:n.*227G>T
NM_001289910.1:c.446G>T , LRG_611t1:c.446G>T	NP_001276839.1:p.Gly149Val
NM_001290114.1:c.212G>T	NP_001277043.1:p.Gly71Val
NM_002168.3:c.602G>T , LRG_611t2:c.602G>T	NP_002159.2:p.Gly201Val
NM_001290114.2:c.212G>T	NP_001277043.1:p.Gly71Val
NM_002168.4:c.602G>T MANE Select	NP_002159.2:p.Gly201Val