Canonical Allele Identifier: CA393802241

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549561
• MyVariant Identifiers: chr15:g.90631841C>G (hg19) ; chr15:g.90088609C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088609C>G , CM000677.2:g.90088609C>G	GRCh38
NC_000015.9:g.90631841C>G , CM000677.1:g.90631841C>G	GRCh37
NC_000015.8:g.88432845C>G	NCBI36
NG_023302.1:g.18868G>C , LRG_611:g.18868G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.512G>C MANE Select	ENSP00000331897.4:p.Gly171Ala
ENST00000330062.7:c.512G>C	ENSP00000331897.3:p.Gly171Ala
ENST00000540499.2:c.356G>C	ENSP00000446147.2:p.Gly119Ala
ENST00000559482.5:c.208-107G>C	ENSP00000453016.1:n.208-107G>C
ENST00000560061.1:c.*137G>C	ENSP00000453254.1:n.*137G>C
NM_001289910.1:c.356G>C , LRG_611t1:c.356G>C	NP_001276839.1:p.Gly119Ala
NM_001290114.1:c.122G>C	NP_001277043.1:p.Gly41Ala
NM_002168.3:c.512G>C , LRG_611t2:c.512G>C	NP_002159.2:p.Gly171Ala
NM_001290114.2:c.122G>C	NP_001277043.1:p.Gly41Ala
NM_002168.4:c.512G>C MANE Select	NP_002159.2:p.Gly171Ala