Canonical Allele Identifier: CA274623361

Gene: IDH2

Linked Data

• dbSNP Id: rs558137284
• gnomAD v3: 15-90088264-G-A
• gnomAD v4: 15-90088264-G-A
• MyVariant Identifiers: chr15:g.90631496G>A (hg19) ; chr15:g.90088264G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088264G>A , CM000677.2:g.90088264G>A	GRCh38
NC_000015.9:g.90631496G>A , CM000677.1:g.90631496G>A	GRCh37
NC_000015.8:g.88432500G>A	NCBI36
NG_023302.1:g.19213C>T , LRG_611:g.19213C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.678+95C>T MANE Select	ENSP00000331897.4:n.678+95C>T
ENST00000330062.7:c.678+95C>T	ENSP00000331897.3:n.678+95C>T
ENST00000540499.2:c.522+95C>T	ENSP00000446147.2:n.522+95C>T
ENST00000559482.5:c.351+95C>T	ENSP00000453016.1:n.351+95C>T
ENST00000560061.1:c.*303+95C>T	ENSP00000453254.1:n.*303+95C>T
NM_001289910.1:c.522+95C>T , LRG_611t1:c.522+95C>T	NP_001276839.1:n.522+95C>T
NM_001290114.1:c.288+95C>T	NP_001277043.1:n.288+95C>T
NM_002168.3:c.678+95C>T , LRG_611t2:c.678+95C>T	NP_002159.2:n.678+95C>T
NM_001290114.2:c.288+95C>T	NP_001277043.1:n.288+95C>T
NM_002168.4:c.678+95C>T MANE Select	NP_002159.2:n.678+95C>T