Canonical Allele Identifier: CA393801954

Gene: IDH2

Linked Data

• MyVariant Identifiers: chr15:g.90631631G>C (hg19) ; chr15:g.90088399G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088399G>C , CM000677.2:g.90088399G>C	GRCh38
NC_000015.9:g.90631631G>C , CM000677.1:g.90631631G>C	GRCh37
NC_000015.8:g.88432635G>C	NCBI36
NG_023302.1:g.19078C>G , LRG_611:g.19078C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.638C>G MANE Select	ENSP00000331897.4:p.Pro213Arg
ENST00000330062.7:c.638C>G	ENSP00000331897.3:p.Pro213Arg
ENST00000540499.2:c.482C>G	ENSP00000446147.2:p.Pro161Arg
ENST00000559482.5:c.311C>G	ENSP00000453016.1:p.Pro104Arg
ENST00000560061.1:c.*263C>G	ENSP00000453254.1:n.*263C>G
NM_001289910.1:c.482C>G , LRG_611t1:c.482C>G	NP_001276839.1:p.Pro161Arg
NM_001290114.1:c.248C>G	NP_001277043.1:p.Pro83Arg
NM_002168.3:c.638C>G , LRG_611t2:c.638C>G	NP_002159.2:p.Pro213Arg
NM_001290114.2:c.248C>G	NP_001277043.1:p.Pro83Arg
NM_002168.4:c.638C>G MANE Select	NP_002159.2:p.Pro213Arg