Canonical Allele Identifier: CA7733160

Gene: IDH2

Linked Data

• dbSNP Id: rs747955566
• ExAC: 15:90631777 G / T
• gnomAD v2: 15-90631777-G-T
• gnomAD v3: 15-90088545-G-T
• gnomAD v4: 15-90088545-G-T
• MyVariant Identifiers: chr15:g.90631777G>T (hg19) ; chr15:g.90088545G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088545G>T , CM000677.2:g.90088545G>T	GRCh38
NC_000015.9:g.90631777G>T , CM000677.1:g.90631777G>T	GRCh37
NC_000015.8:g.88432781G>T	NCBI36
NG_023302.1:g.18932C>A , LRG_611:g.18932C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.535-43C>A MANE Select	ENSP00000331897.4:n.535-43C>A
ENST00000330062.7:c.535-43C>A	ENSP00000331897.3:n.535-43C>A
ENST00000540499.2:c.379-43C>A	ENSP00000446147.2:n.379-43C>A
ENST00000559482.5:c.208-43C>A	ENSP00000453016.1:n.208-43C>A
ENST00000560061.1:c.*160-43C>A	ENSP00000453254.1:n.*160-43C>A
NM_001289910.1:c.379-43C>A , LRG_611t1:c.379-43C>A	NP_001276839.1:n.379-43C>A
NM_001290114.1:c.145-43C>A	NP_001277043.1:n.145-43C>A
NM_002168.3:c.535-43C>A , LRG_611t2:c.535-43C>A	NP_002159.2:n.535-43C>A
NM_001290114.2:c.145-43C>A	NP_001277043.1:n.145-43C>A
NM_002168.4:c.535-43C>A MANE Select	NP_002159.2:n.535-43C>A