Canonical Allele Identifier: CA2630319202

Gene: IDH2

Linked Data

• gnomAD v4: 15-90088285-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088285A>C , CM000677.2:g.90088285A>C	GRCh38
NC_000015.9:g.90631517A>C , CM000677.1:g.90631517A>C	GRCh37
NC_000015.8:g.88432521A>C	NCBI36
NG_023302.1:g.19192T>G , LRG_611:g.19192T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.678+74T>G MANE Select	ENSP00000331897.4:n.678+74T>G
ENST00000330062.7:c.678+74T>G	ENSP00000331897.3:n.678+74T>G
ENST00000540499.2:c.522+74T>G	ENSP00000446147.2:n.522+74T>G
ENST00000559482.5:c.351+74T>G	ENSP00000453016.1:n.351+74T>G
ENST00000560061.1:c.*303+74T>G	ENSP00000453254.1:n.*303+74T>G
NM_001289910.1:c.522+74T>G , LRG_611t1:c.522+74T>G	NP_001276839.1:n.522+74T>G
NM_001290114.1:c.288+74T>G	NP_001277043.1:n.288+74T>G
NM_002168.3:c.678+74T>G , LRG_611t2:c.678+74T>G	NP_002159.2:n.678+74T>G
NM_001290114.2:c.288+74T>G	NP_001277043.1:n.288+74T>G
NM_002168.4:c.678+74T>G MANE Select	NP_002159.2:n.678+74T>G