Canonical Allele Identifier: CA492297424
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs749079848
MyVariant Identifiers: chr15:g.90631624G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088392G>C , CM000677.2:g.90088392G>C GRCh38
NC_000015.9:g.90631624G>C , CM000677.1:g.90631624G>C GRCh37
NC_000015.8:g.88432628G>C NCBI36
NG_023302.1:g.19085C>G , LRG_611:g.19085C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.645C>G MANE Select ENSP00000331897.4:p.Gly215=
ENST00000330062.7:c.645C>G ENSP00000331897.3:p.Gly215=
ENST00000540499.2:c.489C>G ENSP00000446147.2:p.Gly163=
ENST00000559482.5:c.318C>G ENSP00000453016.1:p.Gly106=
ENST00000560061.1:c.*270C>G ENSP00000453254.1:n.*270C>G
NM_001289910.1:c.489C>G , LRG_611t1:c.489C>G NP_001276839.1:p.Gly163=
NM_001290114.1:c.255C>G NP_001277043.1:p.Gly85=
NM_002168.3:c.645C>G , LRG_611t2:c.645C>G NP_002159.2:p.Gly215=
NM_001290114.2:c.255C>G NP_001277043.1:p.Gly85=
NM_002168.4:c.645C>G MANE Select NP_002159.2:p.Gly215=