Canonical Allele Identifier: CA492298103

Gene: IDH2

Linked Data

• dbSNP Id: rs1596074671
• gnomAD v3: 15-90088668-G-A
• gnomAD v4: 15-90088668-G-A
• MyVariant Identifiers: chr15:g.90631900G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088668G>A , CM000677.2:g.90088668G>A	GRCh38
NC_000015.9:g.90631900G>A , CM000677.1:g.90631900G>A	GRCh37
NC_000015.8:g.88432904G>A	NCBI36
NG_023302.1:g.18809C>T , LRG_611:g.18809C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.453C>T MANE Select	ENSP00000331897.4:p.Pro151=
ENST00000330062.7:c.453C>T	ENSP00000331897.3:p.Pro151=
ENST00000540499.2:c.297C>T	ENSP00000446147.2:p.Pro99=
ENST00000559482.5:c.208-166C>T	ENSP00000453016.1:n.208-166C>T
ENST00000560061.1:c.*78C>T	ENSP00000453254.1:n.*78C>T
NM_001289910.1:c.297C>T , LRG_611t1:c.297C>T	NP_001276839.1:p.Pro99=
NM_001290114.1:c.63C>T	NP_001277043.1:p.Pro21=
NM_002168.3:c.453C>T , LRG_611t2:c.453C>T	NP_002159.2:p.Pro151=
NM_001290114.2:c.63C>T	NP_001277043.1:p.Pro21=
NM_002168.4:c.453C>T MANE Select	NP_002159.2:p.Pro151=