Canonical Allele Identifier: CA274623653

Gene: IDH2

Linked Data

• dbSNP Id: rs769450167
• gnomAD v2: 15-90631678-G-C
• gnomAD v4: 15-90088446-G-C
• MyVariant Identifiers: chr15:g.90631678G>C (hg19) ; chr15:g.90088446G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088446G>C , CM000677.2:g.90088446G>C	GRCh38
NC_000015.9:g.90631678G>C , CM000677.1:g.90631678G>C	GRCh37
NC_000015.8:g.88432682G>C	NCBI36
NG_023302.1:g.19031C>G , LRG_611:g.19031C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.591C>G MANE Select	ENSP00000331897.4:p.Thr197=
ENST00000330062.7:c.591C>G	ENSP00000331897.3:p.Thr197=
ENST00000540499.2:c.435C>G	ENSP00000446147.2:p.Thr145=
ENST00000559482.5:c.264C>G	ENSP00000453016.1:p.Thr88=
ENST00000560061.1:c.*216C>G	ENSP00000453254.1:n.*216C>G
NM_001289910.1:c.435C>G , LRG_611t1:c.435C>G	NP_001276839.1:p.Thr145=
NM_001290114.1:c.201C>G	NP_001277043.1:p.Thr67=
NM_002168.3:c.591C>G , LRG_611t2:c.591C>G	NP_002159.2:p.Thr197=
NM_001290114.2:c.201C>G	NP_001277043.1:p.Thr67=
NM_002168.4:c.591C>G MANE Select	NP_002159.2:p.Thr197=