Canonical Allele Identifier: CA393802011
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs1900931461

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088422C>G , CM000677.2:g.90088422C>G GRCh38
NC_000015.9:g.90631654C>G , CM000677.1:g.90631654C>G GRCh37
NC_000015.8:g.88432658C>G NCBI36
NG_023302.1:g.19055G>C , LRG_611:g.19055G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.615G>C MANE Select ENSP00000331897.4:p.Lys205Asn
ENST00000330062.7:c.615G>C ENSP00000331897.3:p.Lys205Asn
ENST00000540499.2:c.459G>C ENSP00000446147.2:p.Lys153Asn
ENST00000559482.5:c.288G>C ENSP00000453016.1:p.Lys96Asn
ENST00000560061.1:c.*240G>C ENSP00000453254.1:n.*240G>C
NM_001289910.1:c.459G>C , LRG_611t1:c.459G>C NP_001276839.1:p.Lys153Asn
NM_001290114.1:c.225G>C NP_001277043.1:p.Lys75Asn
NM_002168.3:c.615G>C , LRG_611t2:c.615G>C NP_002159.2:p.Lys205Asn
NM_001290114.2:c.225G>C NP_001277043.1:p.Lys75Asn
NM_002168.4:c.615G>C MANE Select NP_002159.2:p.Lys205Asn