Canonical Allele Identifier: CA492298046
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs1191538570
MyVariant Identifiers: chr15:g.90631852G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088620G>T , CM000677.2:g.90088620G>T GRCh38
NC_000015.9:g.90631852G>T , CM000677.1:g.90631852G>T GRCh37
NC_000015.8:g.88432856G>T NCBI36
NG_023302.1:g.18857C>A , LRG_611:g.18857C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.501C>A MANE Select ENSP00000331897.4:p.Pro167=
ENST00000330062.7:c.501C>A ENSP00000331897.3:p.Pro167=
ENST00000540499.2:c.345C>A ENSP00000446147.2:p.Pro115=
ENST00000559482.5:c.208-118C>A ENSP00000453016.1:n.208-118C>A
ENST00000560061.1:c.*126C>A ENSP00000453254.1:n.*126C>A
NM_001289910.1:c.345C>A , LRG_611t1:c.345C>A NP_001276839.1:p.Pro115=
NM_001290114.1:c.111C>A NP_001277043.1:p.Pro37=
NM_002168.3:c.501C>A , LRG_611t2:c.501C>A NP_002159.2:p.Pro167=
NM_001290114.2:c.111C>A NP_001277043.1:p.Pro37=
NM_002168.4:c.501C>A MANE Select NP_002159.2:p.Pro167=