Canonical Allele Identifier: CA492297414
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs2151549172
MyVariant Identifiers: chr15:g.90631615G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088383G>A , CM000677.2:g.90088383G>A GRCh38
NC_000015.9:g.90631615G>A , CM000677.1:g.90631615G>A GRCh37
NC_000015.8:g.88432619G>A NCBI36
NG_023302.1:g.19094C>T , LRG_611:g.19094C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.654C>T MANE Select ENSP00000331897.4:p.Gly218=
ENST00000330062.7:c.654C>T ENSP00000331897.3:p.Gly218=
ENST00000540499.2:c.498C>T ENSP00000446147.2:p.Gly166=
ENST00000559482.5:c.327C>T ENSP00000453016.1:p.Gly109=
ENST00000560061.1:c.*279C>T ENSP00000453254.1:n.*279C>T
NM_001289910.1:c.498C>T , LRG_611t1:c.498C>T NP_001276839.1:p.Gly166=
NM_001290114.1:c.264C>T NP_001277043.1:p.Gly88=
NM_002168.3:c.654C>T , LRG_611t2:c.654C>T NP_002159.2:p.Gly218=
NM_001290114.2:c.264C>T NP_001277043.1:p.Gly88=
NM_002168.4:c.654C>T MANE Select NP_002159.2:p.Gly218=