Canonical Allele Identifier: CA393801975
Gene: IDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088407G>T , CM000677.2:g.90088407G>T GRCh38
NC_000015.9:g.90631639G>T , CM000677.1:g.90631639G>T GRCh37
NC_000015.8:g.88432643G>T NCBI36
NG_023302.1:g.19070C>A , LRG_611:g.19070C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.630C>A MANE Select ENSP00000331897.4:p.Tyr210Ter
ENST00000330062.7:c.630C>A ENSP00000331897.3:p.Tyr210Ter
ENST00000540499.2:c.474C>A ENSP00000446147.2:p.Tyr158Ter
ENST00000559482.5:c.303C>A ENSP00000453016.1:p.Tyr101Ter
ENST00000560061.1:c.*255C>A ENSP00000453254.1:n.*255C>A
NM_001289910.1:c.474C>A , LRG_611t1:c.474C>A NP_001276839.1:p.Tyr158Ter
NM_001290114.1:c.240C>A NP_001277043.1:p.Tyr80Ter
NM_002168.3:c.630C>A , LRG_611t2:c.630C>A NP_002159.2:p.Tyr210Ter
NM_001290114.2:c.240C>A NP_001277043.1:p.Tyr80Ter
NM_002168.4:c.630C>A MANE Select NP_002159.2:p.Tyr210Ter