Canonical Allele Identifier: CA2630319338

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549433
• gnomAD v4: 15-90088559-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088559A>G , CM000677.2:g.90088559A>G	GRCh38
NC_000015.9:g.90631791A>G , CM000677.1:g.90631791A>G	GRCh37
NC_000015.8:g.88432795A>G	NCBI36
NG_023302.1:g.18918T>C , LRG_611:g.18918T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.534+28T>C MANE Select	ENSP00000331897.4:n.534+28T>C
ENST00000330062.7:c.534+28T>C	ENSP00000331897.3:n.534+28T>C
ENST00000540499.2:c.378+28T>C	ENSP00000446147.2:n.378+28T>C
ENST00000559482.5:c.208-57T>C	ENSP00000453016.1:n.208-57T>C
ENST00000560061.1:c.*159+28T>C	ENSP00000453254.1:n.*159+28T>C
NM_001289910.1:c.378+28T>C , LRG_611t1:c.378+28T>C	NP_001276839.1:n.378+28T>C
NM_001290114.1:c.144+28T>C	NP_001277043.1:n.144+28T>C
NM_002168.3:c.534+28T>C , LRG_611t2:c.534+28T>C	NP_002159.2:n.534+28T>C
NM_001290114.2:c.144+28T>C	NP_001277043.1:n.144+28T>C
NM_002168.4:c.534+28T>C MANE Select	NP_002159.2:n.534+28T>C