Canonical Allele Identifier: CA393802064

Gene: IDH2

Linked Data

• dbSNP Id: rs1900932649
• gnomAD v3: 15-90088448-T-A
• gnomAD v4: 15-90088448-T-A
• MyVariant Identifiers: chr15:g.90631680T>A (hg19) ; chr15:g.90088448T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088448T>A , CM000677.2:g.90088448T>A	GRCh38
NC_000015.9:g.90631680T>A , CM000677.1:g.90631680T>A	GRCh37
NC_000015.8:g.88432684T>A	NCBI36
NG_023302.1:g.19029A>T , LRG_611:g.19029A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.589A>T MANE Select	ENSP00000331897.4:p.Thr197Ser
ENST00000330062.7:c.589A>T	ENSP00000331897.3:p.Thr197Ser
ENST00000540499.2:c.433A>T	ENSP00000446147.2:p.Thr145Ser
ENST00000559482.5:c.262A>T	ENSP00000453016.1:p.Thr88Ser
ENST00000560061.1:c.*214A>T	ENSP00000453254.1:n.*214A>T
NM_001289910.1:c.433A>T , LRG_611t1:c.433A>T	NP_001276839.1:p.Thr145Ser
NM_001290114.1:c.199A>T	NP_001277043.1:p.Thr67Ser
NM_002168.3:c.589A>T , LRG_611t2:c.589A>T	NP_002159.2:p.Thr197Ser
NM_001290114.2:c.199A>T	NP_001277043.1:p.Thr67Ser
NM_002168.4:c.589A>T MANE Select	NP_002159.2:p.Thr197Ser