Canonical Allele Identifier: CA393802058

Gene: IDH2

Linked Data

• dbSNP Id: rs1900932203
• gnomAD v4: 15-90088444-G-A
• MyVariant Identifiers: chr15:g.90631676G>A (hg19) ; chr15:g.90088444G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088444G>A , CM000677.2:g.90088444G>A	GRCh38
NC_000015.9:g.90631676G>A , CM000677.1:g.90631676G>A	GRCh37
NC_000015.8:g.88432680G>A	NCBI36
NG_023302.1:g.19033C>T , LRG_611:g.19033C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.593C>T MANE Select	ENSP00000331897.4:p.Pro198Leu
ENST00000330062.7:c.593C>T	ENSP00000331897.3:p.Pro198Leu
ENST00000540499.2:c.437C>T	ENSP00000446147.2:p.Pro146Leu
ENST00000559482.5:c.266C>T	ENSP00000453016.1:p.Pro89Leu
ENST00000560061.1:c.*218C>T	ENSP00000453254.1:n.*218C>T
NM_001289910.1:c.437C>T , LRG_611t1:c.437C>T	NP_001276839.1:p.Pro146Leu
NM_001290114.1:c.203C>T	NP_001277043.1:p.Pro68Leu
NM_002168.3:c.593C>T , LRG_611t2:c.593C>T	NP_002159.2:p.Pro198Leu
NM_001290114.2:c.203C>T	NP_001277043.1:p.Pro68Leu
NM_002168.4:c.593C>T MANE Select	NP_002159.2:p.Pro198Leu