Canonical Allele Identifier: CA716980297

Gene: IDH2

Linked Data

• dbSNP Id: rs1483774781
• gnomAD v3: 15-90088796-A-G
• gnomAD v4: 15-90088796-A-G
• MyVariant Identifiers: chr15:g.90632028A>G (hg19) ; chr15:g.90088796A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088796A>G , CM000677.2:g.90088796A>G	GRCh38
NC_000015.9:g.90632028A>G , CM000677.1:g.90632028A>G	GRCh37
NC_000015.8:g.88433032A>G	NCBI36
NG_023302.1:g.18681T>C , LRG_611:g.18681T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.374-49T>C MANE Select	ENSP00000331897.4:n.374-49T>C
ENST00000330062.7:c.374-49T>C	ENSP00000331897.3:n.374-49T>C
ENST00000540499.2:c.218-49T>C	ENSP00000446147.2:n.218-49T>C
ENST00000559482.5:c.208-294T>C	ENSP00000453016.1:n.208-294T>C
ENST00000560061.1:c.116-49T>C	ENSP00000453254.1:n.116-49T>C
NM_001289910.1:c.218-49T>C , LRG_611t1:c.218-49T>C	NP_001276839.1:n.218-49T>C
NM_001290114.1:c.-17-49T>C	NP_001277043.1:n.-17-49T>C
NM_002168.3:c.374-49T>C , LRG_611t2:c.374-49T>C	NP_002159.2:n.374-49T>C
NM_001290114.2:c.-17-49T>C	NP_001277043.1:n.-17-49T>C
NM_002168.4:c.374-49T>C MANE Select	NP_002159.2:n.374-49T>C