Canonical Allele Identifier: CA393801982

Gene: IDH2

Linked Data

• MyVariant Identifiers: chr15:g.90631643A>G (hg19) ; chr15:g.90088411A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088411A>G , CM000677.2:g.90088411A>G	GRCh38
NC_000015.9:g.90631643A>G , CM000677.1:g.90631643A>G	GRCh37
NC_000015.8:g.88432647A>G	NCBI36
NG_023302.1:g.19066T>C , LRG_611:g.19066T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.626T>C MANE Select	ENSP00000331897.4:p.Val209Ala
ENST00000330062.7:c.626T>C	ENSP00000331897.3:p.Val209Ala
ENST00000540499.2:c.470T>C	ENSP00000446147.2:p.Val157Ala
ENST00000559482.5:c.299T>C	ENSP00000453016.1:p.Val100Ala
ENST00000560061.1:c.*251T>C	ENSP00000453254.1:n.*251T>C
NM_001289910.1:c.470T>C , LRG_611t1:c.470T>C	NP_001276839.1:p.Val157Ala
NM_001290114.1:c.236T>C	NP_001277043.1:p.Val79Ala
NM_002168.3:c.626T>C , LRG_611t2:c.626T>C	NP_002159.2:p.Val209Ala
NM_001290114.2:c.236T>C	NP_001277043.1:p.Val79Ala
NM_002168.4:c.626T>C MANE Select	NP_002159.2:p.Val209Ala