Canonical Allele Identifier: CA393801942
Gene: IDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088393C>A , CM000677.2:g.90088393C>A GRCh38
NC_000015.9:g.90631625C>A , CM000677.1:g.90631625C>A GRCh37
NC_000015.8:g.88432629C>A NCBI36
NG_023302.1:g.19084G>T , LRG_611:g.19084G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.644G>T MANE Select ENSP00000331897.4:p.Gly215Val
ENST00000330062.7:c.644G>T ENSP00000331897.3:p.Gly215Val
ENST00000540499.2:c.488G>T ENSP00000446147.2:p.Gly163Val
ENST00000559482.5:c.317G>T ENSP00000453016.1:p.Gly106Val
ENST00000560061.1:c.*269G>T ENSP00000453254.1:n.*269G>T
NM_001289910.1:c.488G>T , LRG_611t1:c.488G>T NP_001276839.1:p.Gly163Val
NM_001290114.1:c.254G>T NP_001277043.1:p.Gly85Val
NM_002168.3:c.644G>T , LRG_611t2:c.644G>T NP_002159.2:p.Gly215Val
NM_001290114.2:c.254G>T NP_001277043.1:p.Gly85Val
NM_002168.4:c.644G>T MANE Select NP_002159.2:p.Gly215Val