Canonical Allele Identifier: CA393802436

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549794
• MyVariant Identifiers: chr15:g.90631937A>T (hg19) ; chr15:g.90088705A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088705A>T , CM000677.2:g.90088705A>T	GRCh38
NC_000015.9:g.90631937A>T , CM000677.1:g.90631937A>T	GRCh37
NC_000015.8:g.88432941A>T	NCBI36
NG_023302.1:g.18772T>A , LRG_611:g.18772T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.416T>A MANE Select	ENSP00000331897.4:p.Ile139Asn
ENST00000330062.7:c.416T>A	ENSP00000331897.3:p.Ile139Asn
ENST00000540499.2:c.260T>A	ENSP00000446147.2:p.Ile87Asn
ENST00000559482.5:c.208-203T>A	ENSP00000453016.1:n.208-203T>A
ENST00000560061.1:c.*41T>A	ENSP00000453254.1:n.*41T>A
NM_001289910.1:c.260T>A , LRG_611t1:c.260T>A	NP_001276839.1:p.Ile87Asn
NM_001290114.1:c.26T>A	NP_001277043.1:p.Ile9Asn
NM_002168.3:c.416T>A , LRG_611t2:c.416T>A	NP_002159.2:p.Ile139Asn
NM_001290114.2:c.26T>A	NP_001277043.1:p.Ile9Asn
NM_002168.4:c.416T>A MANE Select	NP_002159.2:p.Ile139Asn