Canonical Allele Identifier: CA393802338

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549668
• MyVariant Identifiers: chr15:g.90631887T>C (hg19) ; chr15:g.90088655T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088655T>C , CM000677.2:g.90088655T>C	GRCh38
NC_000015.9:g.90631887T>C , CM000677.1:g.90631887T>C	GRCh37
NC_000015.8:g.88432891T>C	NCBI36
NG_023302.1:g.18822A>G , LRG_611:g.18822A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.466A>G MANE Select	ENSP00000331897.4:p.Asn156Asp
ENST00000330062.7:c.466A>G	ENSP00000331897.3:p.Asn156Asp
ENST00000540499.2:c.310A>G	ENSP00000446147.2:p.Asn104Asp
ENST00000559482.5:c.208-153A>G	ENSP00000453016.1:n.208-153A>G
ENST00000560061.1:c.*91A>G	ENSP00000453254.1:n.*91A>G
NM_001289910.1:c.310A>G , LRG_611t1:c.310A>G	NP_001276839.1:p.Asn104Asp
NM_001290114.1:c.76A>G	NP_001277043.1:p.Asn26Asp
NM_002168.3:c.466A>G , LRG_611t2:c.466A>G	NP_002159.2:p.Asn156Asp
NM_001290114.2:c.76A>G	NP_001277043.1:p.Asn26Asp
NM_002168.4:c.466A>G MANE Select	NP_002159.2:p.Asn156Asp