Canonical Allele Identifier: CA393802070

Gene: IDH2

Linked Data

• MyVariant Identifiers: chr15:g.90631682A>G (hg19) ; chr15:g.90088450A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088450A>G , CM000677.2:g.90088450A>G	GRCh38
NC_000015.9:g.90631682A>G , CM000677.1:g.90631682A>G	GRCh37
NC_000015.8:g.88432686A>G	NCBI36
NG_023302.1:g.19027T>C , LRG_611:g.19027T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.587T>C MANE Select	ENSP00000331897.4:p.Phe196Ser
ENST00000330062.7:c.587T>C	ENSP00000331897.3:p.Phe196Ser
ENST00000540499.2:c.431T>C	ENSP00000446147.2:p.Phe144Ser
ENST00000559482.5:c.260T>C	ENSP00000453016.1:p.Phe87Ser
ENST00000560061.1:c.*212T>C	ENSP00000453254.1:n.*212T>C
NM_001289910.1:c.431T>C , LRG_611t1:c.431T>C	NP_001276839.1:p.Phe144Ser
NM_001290114.1:c.197T>C	NP_001277043.1:p.Phe66Ser
NM_002168.3:c.587T>C , LRG_611t2:c.587T>C	NP_002159.2:p.Phe196Ser
NM_001290114.2:c.197T>C	NP_001277043.1:p.Phe66Ser
NM_002168.4:c.587T>C MANE Select	NP_002159.2:p.Phe196Ser