Canonical Allele Identifier: CA393801947
Gene: IDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088394C>T , CM000677.2:g.90088394C>T GRCh38
NC_000015.9:g.90631626C>T , CM000677.1:g.90631626C>T GRCh37
NC_000015.8:g.88432630C>T NCBI36
NG_023302.1:g.19083G>A , LRG_611:g.19083G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.643G>A MANE Select ENSP00000331897.4:p.Gly215Ser
ENST00000330062.7:c.643G>A ENSP00000331897.3:p.Gly215Ser
ENST00000540499.2:c.487G>A ENSP00000446147.2:p.Gly163Ser
ENST00000559482.5:c.316G>A ENSP00000453016.1:p.Gly106Ser
ENST00000560061.1:c.*268G>A ENSP00000453254.1:n.*268G>A
NM_001289910.1:c.487G>A , LRG_611t1:c.487G>A NP_001276839.1:p.Gly163Ser
NM_001290114.1:c.253G>A NP_001277043.1:p.Gly85Ser
NM_002168.3:c.643G>A , LRG_611t2:c.643G>A NP_002159.2:p.Gly215Ser
NM_001290114.2:c.253G>A NP_001277043.1:p.Gly85Ser
NM_002168.4:c.643G>A MANE Select NP_002159.2:p.Gly215Ser