Canonical Allele Identifier: CA393802300

Gene: IDH2

Linked Data

• dbSNP Id: rs1382680247
• COSMIC: COSM1736930
• MyVariant Identifiers: chr15:g.90631869G>A (hg19) ; chr15:g.90088637G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088637G>A , CM000677.2:g.90088637G>A	GRCh38
NC_000015.9:g.90631869G>A , CM000677.1:g.90631869G>A	GRCh37
NC_000015.8:g.88432873G>A	NCBI36
NG_023302.1:g.18840C>T , LRG_611:g.18840C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.484C>T MANE Select	ENSP00000331897.4:p.Pro162Ser
ENST00000330062.7:c.484C>T	ENSP00000331897.3:p.Pro162Ser
ENST00000540499.2:c.328C>T	ENSP00000446147.2:p.Pro110Ser
ENST00000559482.5:c.208-135C>T	ENSP00000453016.1:n.208-135C>T
ENST00000560061.1:c.*109C>T	ENSP00000453254.1:n.*109C>T
NM_001289910.1:c.328C>T , LRG_611t1:c.328C>T	NP_001276839.1:p.Pro110Ser
NM_001290114.1:c.94C>T	NP_001277043.1:p.Pro32Ser
NM_002168.3:c.484C>T , LRG_611t2:c.484C>T	NP_002159.2:p.Pro162Ser
NM_001290114.2:c.94C>T	NP_001277043.1:p.Pro32Ser
NM_002168.4:c.484C>T MANE Select	NP_002159.2:p.Pro162Ser