Canonical Allele Identifier: CA2630319219

Gene: IDH2

Linked Data

• gnomAD v4: 15-90088323-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088323G>A , CM000677.2:g.90088323G>A	GRCh38
NC_000015.9:g.90631555G>A , CM000677.1:g.90631555G>A	GRCh37
NC_000015.8:g.88432559G>A	NCBI36
NG_023302.1:g.19154C>T , LRG_611:g.19154C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.678+36C>T MANE Select	ENSP00000331897.4:n.678+36C>T
ENST00000330062.7:c.678+36C>T	ENSP00000331897.3:n.678+36C>T
ENST00000540499.2:c.522+36C>T	ENSP00000446147.2:n.522+36C>T
ENST00000559482.5:c.351+36C>T	ENSP00000453016.1:n.351+36C>T
ENST00000560061.1:c.*303+36C>T	ENSP00000453254.1:n.*303+36C>T
NM_001289910.1:c.522+36C>T , LRG_611t1:c.522+36C>T	NP_001276839.1:n.522+36C>T
NM_001290114.1:c.288+36C>T	NP_001277043.1:n.288+36C>T
NM_002168.3:c.678+36C>T , LRG_611t2:c.678+36C>T	NP_002159.2:n.678+36C>T
NM_001290114.2:c.288+36C>T	NP_001277043.1:n.288+36C>T
NM_002168.4:c.678+36C>T MANE Select	NP_002159.2:n.678+36C>T