Canonical Allele Identifier: CA492297405
Gene: IDH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.90631609G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088377G>T , CM000677.2:g.90088377G>T GRCh38
NC_000015.9:g.90631609G>T , CM000677.1:g.90631609G>T GRCh37
NC_000015.8:g.88432613G>T NCBI36
NG_023302.1:g.19100C>A , LRG_611:g.19100C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.660C>A MANE Select ENSP00000331897.4:p.Gly220=
ENST00000330062.7:c.660C>A ENSP00000331897.3:p.Gly220=
ENST00000540499.2:c.504C>A ENSP00000446147.2:p.Gly168=
ENST00000559482.5:c.333C>A ENSP00000453016.1:p.Gly111=
ENST00000560061.1:c.*285C>A ENSP00000453254.1:n.*285C>A
NM_001289910.1:c.504C>A , LRG_611t1:c.504C>A NP_001276839.1:p.Gly168=
NM_001290114.1:c.270C>A NP_001277043.1:p.Gly90=
NM_002168.3:c.660C>A , LRG_611t2:c.660C>A NP_002159.2:p.Gly220=
NM_001290114.2:c.270C>A NP_001277043.1:p.Gly90=
NM_002168.4:c.660C>A MANE Select NP_002159.2:p.Gly220=