Canonical Allele Identifier: CA393802393

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549727
• MyVariant Identifiers: chr15:g.90631911A>T (hg19) ; chr15:g.90088679A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088679A>T , CM000677.2:g.90088679A>T	GRCh38
NC_000015.9:g.90631911A>T , CM000677.1:g.90631911A>T	GRCh37
NC_000015.8:g.88432915A>T	NCBI36
NG_023302.1:g.18798T>A , LRG_611:g.18798T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.442T>A MANE Select	ENSP00000331897.4:p.Phe148Ile
ENST00000330062.7:c.442T>A	ENSP00000331897.3:p.Phe148Ile
ENST00000540499.2:c.286T>A	ENSP00000446147.2:p.Phe96Ile
ENST00000559482.5:c.208-177T>A	ENSP00000453016.1:n.208-177T>A
ENST00000560061.1:c.*67T>A	ENSP00000453254.1:n.*67T>A
NM_001289910.1:c.286T>A , LRG_611t1:c.286T>A	NP_001276839.1:p.Phe96Ile
NM_001290114.1:c.52T>A	NP_001277043.1:p.Phe18Ile
NM_002168.3:c.442T>A , LRG_611t2:c.442T>A	NP_002159.2:p.Phe148Ile
NM_001290114.2:c.52T>A	NP_001277043.1:p.Phe18Ile
NM_002168.4:c.442T>A MANE Select	NP_002159.2:p.Phe148Ile