Canonical Allele Identifier: CA274624224

Gene: IDH2

Linked Data

• dbSNP Id: rs1050541875
• gnomAD v4: 15-90088839-C-A
• MyVariant Identifiers: chr15:g.90632071C>A (hg19) ; chr15:g.90088839C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088839C>A , CM000677.2:g.90088839C>A	GRCh38
NC_000015.9:g.90632071C>A , CM000677.1:g.90632071C>A	GRCh37
NC_000015.8:g.88433075C>A	NCBI36
NG_023302.1:g.18638G>T , LRG_611:g.18638G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.374-92G>T MANE Select	ENSP00000331897.4:n.374-92G>T
ENST00000330062.7:c.374-92G>T	ENSP00000331897.3:n.374-92G>T
ENST00000540499.2:c.218-92G>T	ENSP00000446147.2:n.218-92G>T
ENST00000559482.5:c.208-337G>T	ENSP00000453016.1:n.208-337G>T
ENST00000560061.1:c.116-92G>T	ENSP00000453254.1:n.116-92G>T
NM_001289910.1:c.218-92G>T , LRG_611t1:c.218-92G>T	NP_001276839.1:n.218-92G>T
NM_001290114.1:c.-17-92G>T	NP_001277043.1:n.-17-92G>T
NM_002168.3:c.374-92G>T , LRG_611t2:c.374-92G>T	NP_002159.2:n.374-92G>T
NM_001290114.2:c.-17-92G>T	NP_001277043.1:n.-17-92G>T
NM_002168.4:c.374-92G>T MANE Select	NP_002159.2:n.374-92G>T