Canonical Allele Identifier: CA393801968

Gene: IDH2

Linked Data

• dbSNP Id: rs1163489689
• MyVariant Identifiers: chr15:g.90631637T>A (hg19) ; chr15:g.90088405T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088405T>A , CM000677.2:g.90088405T>A	GRCh38
NC_000015.9:g.90631637T>A , CM000677.1:g.90631637T>A	GRCh37
NC_000015.8:g.88432641T>A	NCBI36
NG_023302.1:g.19072A>T , LRG_611:g.19072A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.632A>T MANE Select	ENSP00000331897.4:p.Asn211Ile
ENST00000330062.7:c.632A>T	ENSP00000331897.3:p.Asn211Ile
ENST00000540499.2:c.476A>T	ENSP00000446147.2:p.Asn159Ile
ENST00000559482.5:c.305A>T	ENSP00000453016.1:p.Asn102Ile
ENST00000560061.1:c.*257A>T	ENSP00000453254.1:n.*257A>T
NM_001289910.1:c.476A>T , LRG_611t1:c.476A>T	NP_001276839.1:p.Asn159Ile
NM_001290114.1:c.242A>T	NP_001277043.1:p.Asn81Ile
NM_002168.3:c.632A>T , LRG_611t2:c.632A>T	NP_002159.2:p.Asn211Ile
NM_001290114.2:c.242A>T	NP_001277043.1:p.Asn81Ile
NM_002168.4:c.632A>T MANE Select	NP_002159.2:p.Asn211Ile