Canonical Allele Identifier: CA492298017
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs2151549542
MyVariant Identifiers: chr15:g.90631831G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088599G>A , CM000677.2:g.90088599G>A GRCh38
NC_000015.9:g.90631831G>A , CM000677.1:g.90631831G>A GRCh37
NC_000015.8:g.88432835G>A NCBI36
NG_023302.1:g.18878C>T , LRG_611:g.18878C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.522C>T MANE Select ENSP00000331897.4:p.Ala174=
ENST00000330062.7:c.522C>T ENSP00000331897.3:p.Ala174=
ENST00000540499.2:c.366C>T ENSP00000446147.2:p.Ala122=
ENST00000559482.5:c.208-97C>T ENSP00000453016.1:n.208-97C>T
ENST00000560061.1:c.*147C>T ENSP00000453254.1:n.*147C>T
NM_001289910.1:c.366C>T , LRG_611t1:c.366C>T NP_001276839.1:p.Ala122=
NM_001290114.1:c.132C>T NP_001277043.1:p.Ala44=
NM_002168.3:c.522C>T , LRG_611t2:c.522C>T NP_002159.2:p.Ala174=
NM_001290114.2:c.132C>T NP_001277043.1:p.Ala44=
NM_002168.4:c.522C>T MANE Select NP_002159.2:p.Ala174=