Canonical Allele Identifier: CA393801918
Gene: IDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088379C>T , CM000677.2:g.90088379C>T GRCh38
NC_000015.9:g.90631611C>T , CM000677.1:g.90631611C>T GRCh37
NC_000015.8:g.88432615C>T NCBI36
NG_023302.1:g.19098G>A , LRG_611:g.19098G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.658G>A MANE Select ENSP00000331897.4:p.Gly220Ser
ENST00000330062.7:c.658G>A ENSP00000331897.3:p.Gly220Ser
ENST00000540499.2:c.502G>A ENSP00000446147.2:p.Gly168Ser
ENST00000559482.5:c.331G>A ENSP00000453016.1:p.Gly111Ser
ENST00000560061.1:c.*283G>A ENSP00000453254.1:n.*283G>A
NM_001289910.1:c.502G>A , LRG_611t1:c.502G>A NP_001276839.1:p.Gly168Ser
NM_001290114.1:c.268G>A NP_001277043.1:p.Gly90Ser
NM_002168.3:c.658G>A , LRG_611t2:c.658G>A NP_002159.2:p.Gly220Ser
NM_001290114.2:c.268G>A NP_001277043.1:p.Gly90Ser
NM_002168.4:c.658G>A MANE Select NP_002159.2:p.Gly220Ser