Canonical Allele Identifier: CA492298067

Gene: IDH2

Linked Data

• MyVariant Identifiers: chr15:g.90631873T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088641T>G , CM000677.2:g.90088641T>G	GRCh38
NC_000015.9:g.90631873T>G , CM000677.1:g.90631873T>G	GRCh37
NC_000015.8:g.88432877T>G	NCBI36
NG_023302.1:g.18836A>C , LRG_611:g.18836A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.480A>C MANE Select	ENSP00000331897.4:p.Leu160=
ENST00000330062.7:c.480A>C	ENSP00000331897.3:p.Leu160=
ENST00000540499.2:c.324A>C	ENSP00000446147.2:p.Leu108=
ENST00000559482.5:c.208-139A>C	ENSP00000453016.1:n.208-139A>C
ENST00000560061.1:c.*105A>C	ENSP00000453254.1:n.*105A>C
NM_001289910.1:c.324A>C , LRG_611t1:c.324A>C	NP_001276839.1:p.Leu108=
NM_001290114.1:c.90A>C	NP_001277043.1:p.Leu30=
NM_002168.3:c.480A>C , LRG_611t2:c.480A>C	NP_002159.2:p.Leu160=
NM_001290114.2:c.90A>C	NP_001277043.1:p.Leu30=
NM_002168.4:c.480A>C MANE Select	NP_002159.2:p.Leu160=