Canonical Allele Identifier: CA492297425
Gene: IDH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.90631624G>T (hg19)

Genomic Alleles

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

Transcript Alleles

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