Canonical Allele Identifier: CA393801979

Gene: IDH2

Linked Data

• MyVariant Identifiers: chr15:g.90631641A>C (hg19) ; chr15:g.90088409A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088409A>C , CM000677.2:g.90088409A>C	GRCh38
NC_000015.9:g.90631641A>C , CM000677.1:g.90631641A>C	GRCh37
NC_000015.8:g.88432645A>C	NCBI36
NG_023302.1:g.19068T>G , LRG_611:g.19068T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.628T>G MANE Select	ENSP00000331897.4:p.Tyr210Asp
ENST00000330062.7:c.628T>G	ENSP00000331897.3:p.Tyr210Asp
ENST00000540499.2:c.472T>G	ENSP00000446147.2:p.Tyr158Asp
ENST00000559482.5:c.301T>G	ENSP00000453016.1:p.Tyr101Asp
ENST00000560061.1:c.*253T>G	ENSP00000453254.1:n.*253T>G
NM_001289910.1:c.472T>G , LRG_611t1:c.472T>G	NP_001276839.1:p.Tyr158Asp
NM_001290114.1:c.238T>G	NP_001277043.1:p.Tyr80Asp
NM_002168.3:c.628T>G , LRG_611t2:c.628T>G	NP_002159.2:p.Tyr210Asp
NM_001290114.2:c.238T>G	NP_001277043.1:p.Tyr80Asp
NM_002168.4:c.628T>G MANE Select	NP_002159.2:p.Tyr210Asp