Canonical Allele Identifier: CA393801948

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549188
• COSMIC: COSM1493548
• MyVariant Identifiers: chr15:g.90631628G>A (hg19) ; chr15:g.90088396G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088396G>A , CM000677.2:g.90088396G>A	GRCh38
NC_000015.9:g.90631628G>A , CM000677.1:g.90631628G>A	GRCh37
NC_000015.8:g.88432632G>A	NCBI36
NG_023302.1:g.19081C>T , LRG_611:g.19081C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.641C>T MANE Select	ENSP00000331897.4:p.Ala214Val
ENST00000330062.7:c.641C>T	ENSP00000331897.3:p.Ala214Val
ENST00000540499.2:c.485C>T	ENSP00000446147.2:p.Ala162Val
ENST00000559482.5:c.314C>T	ENSP00000453016.1:p.Ala105Val
ENST00000560061.1:c.*266C>T	ENSP00000453254.1:n.*266C>T
NM_001289910.1:c.485C>T , LRG_611t1:c.485C>T	NP_001276839.1:p.Ala162Val
NM_001290114.1:c.251C>T	NP_001277043.1:p.Ala84Val
NM_002168.3:c.641C>T , LRG_611t2:c.641C>T	NP_002159.2:p.Ala214Val
NM_001290114.2:c.251C>T	NP_001277043.1:p.Ala84Val
NM_002168.4:c.641C>T MANE Select	NP_002159.2:p.Ala214Val