Canonical Allele Identifier: CA619547906

Gene: IDH2

Linked Data

• dbSNP Id: rs1484714243
• gnomAD v2: 15-90632091-A-G
• gnomAD v3: 15-90088859-A-G
• gnomAD v4: 15-90088859-A-G
• MyVariant Identifiers: chr15:g.90632091A>G (hg19) ; chr15:g.90088859A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088859A>G , CM000677.2:g.90088859A>G	GRCh38
NC_000015.9:g.90632091A>G , CM000677.1:g.90632091A>G	GRCh37
NC_000015.8:g.88433095A>G	NCBI36
NG_023302.1:g.18618T>C , LRG_611:g.18618T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.374-112T>C MANE Select	ENSP00000331897.4:n.374-112T>C
ENST00000330062.7:c.374-112T>C	ENSP00000331897.3:n.374-112T>C
ENST00000540499.2:c.218-112T>C	ENSP00000446147.2:n.218-112T>C
ENST00000559482.5:c.208-357T>C	ENSP00000453016.1:n.208-357T>C
ENST00000560061.1:c.116-112T>C	ENSP00000453254.1:n.116-112T>C
NM_001289910.1:c.218-112T>C , LRG_611t1:c.218-112T>C	NP_001276839.1:n.218-112T>C
NM_001290114.1:c.-17-112T>C	NP_001277043.1:n.-17-112T>C
NM_002168.3:c.374-112T>C , LRG_611t2:c.374-112T>C	NP_002159.2:n.374-112T>C
NM_001290114.2:c.-17-112T>C	NP_001277043.1:n.-17-112T>C
NM_002168.4:c.374-112T>C MANE Select	NP_002159.2:n.374-112T>C