Canonical Allele Identifier: CA393802205

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549514
• MyVariant Identifiers: chr15:g.90631823T>C (hg19) ; chr15:g.90088591T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088591T>C , CM000677.2:g.90088591T>C	GRCh38
NC_000015.9:g.90631823T>C , CM000677.1:g.90631823T>C	GRCh37
NC_000015.8:g.88432827T>C	NCBI36
NG_023302.1:g.18886A>G , LRG_611:g.18886A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.530A>G MANE Select	ENSP00000331897.4:p.Asp177Gly
ENST00000330062.7:c.530A>G	ENSP00000331897.3:p.Asp177Gly
ENST00000540499.2:c.374A>G	ENSP00000446147.2:p.Asp125Gly
ENST00000559482.5:c.208-89A>G	ENSP00000453016.1:n.208-89A>G
ENST00000560061.1:c.*155A>G	ENSP00000453254.1:n.*155A>G
NM_001289910.1:c.374A>G , LRG_611t1:c.374A>G	NP_001276839.1:p.Asp125Gly
NM_001290114.1:c.140A>G	NP_001277043.1:p.Asp47Gly
NM_002168.3:c.530A>G , LRG_611t2:c.530A>G	NP_002159.2:p.Asp177Gly
NM_001290114.2:c.140A>G	NP_001277043.1:p.Asp47Gly
NM_002168.4:c.530A>G MANE Select	NP_002159.2:p.Asp177Gly