Canonical Allele Identifier: CA393802432

Gene: IDH2

Linked Data

• dbSNP Id: rs121913502
• MyVariant Identifiers: chr15:g.90631934C>G (hg19) ; chr15:g.90088702C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088702C>G , CM000677.2:g.90088702C>G	GRCh38
NC_000015.9:g.90631934C>G , CM000677.1:g.90631934C>G	GRCh37
NC_000015.8:g.88432938C>G	NCBI36
NG_023302.1:g.18775G>C , LRG_611:g.18775G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000330062.8:c.419G>C MANE Select	ENSP00000331897.4:p.Arg140Pro
ENST00000330062.7:c.419G>C	ENSP00000331897.3:p.Arg140Pro
ENST00000540499.2:c.263G>C	ENSP00000446147.2:p.Arg88Pro
ENST00000559482.5:c.208-200G>C	ENSP00000453016.1:n.208-200G>C
ENST00000560061.1:c.*44G>C	ENSP00000453254.1:n.*44G>C
NM_001289910.1:c.263G>C , LRG_611t1:c.263G>C	NP_001276839.1:p.Arg88Pro
NM_001290114.1:c.29G>C	NP_001277043.1:p.Arg10Pro
NM_002168.3:c.419G>C , LRG_611t2:c.419G>C	NP_002159.2:p.Arg140Pro
NM_001290114.2:c.29G>C	NP_001277043.1:p.Arg10Pro
NM_002168.4:c.419G>C MANE Select	NP_002159.2:p.Arg140Pro