Canonical Allele Identifier: CA393802502
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs144978761

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088733T>C , CM000677.2:g.90088733T>C GRCh38
NC_000015.9:g.90631965T>C , CM000677.1:g.90631965T>C GRCh37
NC_000015.8:g.88432969T>C NCBI36
NG_023302.1:g.18744A>G , LRG_611:g.18744A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.388A>G MANE Select ENSP00000331897.4:p.Lys130Glu
ENST00000330062.7:c.388A>G ENSP00000331897.3:p.Lys130Glu
ENST00000540499.2:c.232A>G ENSP00000446147.2:p.Lys78Glu
ENST00000559482.5:c.208-231A>G ENSP00000453016.1:n.208-231A>G
ENST00000560061.1:c.*13A>G ENSP00000453254.1:n.*13A>G
NM_001289910.1:c.232A>G , LRG_611t1:c.232A>G NP_001276839.1:p.Lys78Glu
NM_001290114.1:c.-3A>G NP_001277043.1:n.-3A>G
NM_002168.3:c.388A>G , LRG_611t2:c.388A>G NP_002159.2:p.Lys130Glu
NM_001290114.2:c.-3A>G NP_001277043.1:n.-3A>G
NM_002168.4:c.388A>G MANE Select NP_002159.2:p.Lys130Glu