Canonical Allele Identifier: CA619859363

Gene: IDH2

Linked Data

• dbSNP Id: rs1338437488
• gnomAD v2: 15-90631798-C-G
• gnomAD v4: 15-90088566-C-G
• MyVariant Identifiers: chr15:g.90631798C>G (hg19) ; chr15:g.90088566C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088566C>G , CM000677.2:g.90088566C>G	GRCh38
NC_000015.9:g.90631798C>G , CM000677.1:g.90631798C>G	GRCh37
NC_000015.8:g.88432802C>G	NCBI36
NG_023302.1:g.18911G>C , LRG_611:g.18911G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.534+21G>C MANE Select	ENSP00000331897.4:n.534+21G>C
ENST00000330062.7:c.534+21G>C	ENSP00000331897.3:n.534+21G>C
ENST00000540499.2:c.378+21G>C	ENSP00000446147.2:n.378+21G>C
ENST00000559482.5:c.208-64G>C	ENSP00000453016.1:n.208-64G>C
ENST00000560061.1:c.*159+21G>C	ENSP00000453254.1:n.*159+21G>C
NM_001289910.1:c.378+21G>C , LRG_611t1:c.378+21G>C	NP_001276839.1:n.378+21G>C
NM_001290114.1:c.144+21G>C	NP_001277043.1:n.144+21G>C
NM_002168.3:c.534+21G>C , LRG_611t2:c.534+21G>C	NP_002159.2:n.534+21G>C
NM_001290114.2:c.144+21G>C	NP_001277043.1:n.144+21G>C
NM_002168.4:c.534+21G>C MANE Select	NP_002159.2:n.534+21G>C