Canonical Allele Identifier: CA2731565731
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs2151550163

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088829A>G , CM000677.2:g.90088829A>G GRCh38
NC_000015.9:g.90632061A>G , CM000677.1:g.90632061A>G GRCh37
NC_000015.8:g.88433065A>G NCBI36
NG_023302.1:g.18648T>C , LRG_611:g.18648T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.374-82T>C MANE Select ENSP00000331897.4:n.374-82T>C
ENST00000330062.7:c.374-82T>C ENSP00000331897.3:n.374-82T>C
ENST00000540499.2:c.218-82T>C ENSP00000446147.2:n.218-82T>C
ENST00000559482.5:c.208-327T>C ENSP00000453016.1:n.208-327T>C
ENST00000560061.1:c.116-82T>C ENSP00000453254.1:n.116-82T>C
NM_001289910.1:c.218-82T>C , LRG_611t1:c.218-82T>C NP_001276839.1:n.218-82T>C
NM_001290114.1:c.-17-82T>C NP_001277043.1:n.-17-82T>C
NM_002168.3:c.374-82T>C , LRG_611t2:c.374-82T>C NP_002159.2:n.374-82T>C
NM_001290114.2:c.-17-82T>C NP_001277043.1:n.-17-82T>C
NM_002168.4:c.374-82T>C MANE Select NP_002159.2:n.374-82T>C