Canonical Allele Identifier: CA274623570

Gene: IDH2

Linked Data

• dbSNP Id: rs1013298675
• gnomAD v2: 15-90631614-T-C
• gnomAD v3: 15-90088382-T-C
• gnomAD v4: 15-90088382-T-C
• MyVariant Identifiers: chr15:g.90631614T>C (hg19) ; chr15:g.90088382T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088382T>C , CM000677.2:g.90088382T>C	GRCh38
NC_000015.9:g.90631614T>C , CM000677.1:g.90631614T>C	GRCh37
NC_000015.8:g.88432618T>C	NCBI36
NG_023302.1:g.19095A>G , LRG_611:g.19095A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.655A>G MANE Select	ENSP00000331897.4:p.Met219Val
ENST00000330062.7:c.655A>G	ENSP00000331897.3:p.Met219Val
ENST00000540499.2:c.499A>G	ENSP00000446147.2:p.Met167Val
ENST00000559482.5:c.328A>G	ENSP00000453016.1:p.Met110Val
ENST00000560061.1:c.*280A>G	ENSP00000453254.1:n.*280A>G
NM_001289910.1:c.499A>G , LRG_611t1:c.499A>G	NP_001276839.1:p.Met167Val
NM_001290114.1:c.265A>G	NP_001277043.1:p.Met89Val
NM_002168.3:c.655A>G , LRG_611t2:c.655A>G	NP_002159.2:p.Met219Val
NM_001290114.2:c.265A>G	NP_001277043.1:p.Met89Val
NM_002168.4:c.655A>G MANE Select	NP_002159.2:p.Met219Val