Canonical Allele Identifier: CA492297964

Gene: IDH2

Linked Data

• gnomAD v4: 15-90088482-C-T
• MyVariant Identifiers: chr15:g.90631714C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088482C>T , CM000677.2:g.90088482C>T	GRCh38
NC_000015.9:g.90631714C>T , CM000677.1:g.90631714C>T	GRCh37
NC_000015.8:g.88432718C>T	NCBI36
NG_023302.1:g.18995G>A , LRG_611:g.18995G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.555G>A MANE Select	ENSP00000331897.4:p.Val185=
ENST00000330062.7:c.555G>A	ENSP00000331897.3:p.Val185=
ENST00000540499.2:c.399G>A	ENSP00000446147.2:p.Val133=
ENST00000559482.5:c.228G>A	ENSP00000453016.1:p.Val76=
ENST00000560061.1:c.*180G>A	ENSP00000453254.1:n.*180G>A
NM_001289910.1:c.399G>A , LRG_611t1:c.399G>A	NP_001276839.1:p.Val133=
NM_001290114.1:c.165G>A	NP_001277043.1:p.Val55=
NM_002168.3:c.555G>A , LRG_611t2:c.555G>A	NP_002159.2:p.Val185=
NM_001290114.2:c.165G>A	NP_001277043.1:p.Val55=
NM_002168.4:c.555G>A MANE Select	NP_002159.2:p.Val185=