Canonical Allele Identifier: CA492113139
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs2151549909
MyVariant Identifiers: chr15:g.90631969C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088737C>T , CM000677.2:g.90088737C>T GRCh38
NC_000015.9:g.90631969C>T , CM000677.1:g.90631969C>T GRCh37
NC_000015.8:g.88432973C>T NCBI36
NG_023302.1:g.18740G>A , LRG_611:g.18740G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.384G>A MANE Select ENSP00000331897.4:p.Leu128=
ENST00000330062.7:c.384G>A ENSP00000331897.3:p.Leu128=
ENST00000540499.2:c.228G>A ENSP00000446147.2:p.Leu76=
ENST00000559482.5:c.208-235G>A ENSP00000453016.1:n.208-235G>A
ENST00000560061.1:c.*9G>A ENSP00000453254.1:n.*9G>A
NM_001289910.1:c.228G>A , LRG_611t1:c.228G>A NP_001276839.1:p.Leu76=
NM_001290114.1:c.-7G>A NP_001277043.1:n.-7G>A
NM_002168.3:c.384G>A , LRG_611t2:c.384G>A NP_002159.2:p.Leu128=
NM_001290114.2:c.-7G>A NP_001277043.1:n.-7G>A
NM_002168.4:c.384G>A MANE Select NP_002159.2:p.Leu128=