Canonical Allele Identifier: CA2731242660
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs551828589

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088814A>T , CM000677.2:g.90088814A>T GRCh38
NC_000015.9:g.90632046A>T , CM000677.1:g.90632046A>T GRCh37
NC_000015.8:g.88433050A>T NCBI36
NG_023302.1:g.18663T>A , LRG_611:g.18663T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.374-67T>A MANE Select ENSP00000331897.4:n.374-67T>A
ENST00000330062.7:c.374-67T>A ENSP00000331897.3:n.374-67T>A
ENST00000540499.2:c.218-67T>A ENSP00000446147.2:n.218-67T>A
ENST00000559482.5:c.208-312T>A ENSP00000453016.1:n.208-312T>A
ENST00000560061.1:c.116-67T>A ENSP00000453254.1:n.116-67T>A
NM_001289910.1:c.218-67T>A , LRG_611t1:c.218-67T>A NP_001276839.1:n.218-67T>A
NM_001290114.1:c.-17-67T>A NP_001277043.1:n.-17-67T>A
NM_002168.3:c.374-67T>A , LRG_611t2:c.374-67T>A NP_002159.2:n.374-67T>A
NM_001290114.2:c.-17-67T>A NP_001277043.1:n.-17-67T>A
NM_002168.4:c.374-67T>A MANE Select NP_002159.2:n.374-67T>A