Canonical Allele Identifier: CA393801969

Gene: IDH2

Linked Data

• gnomAD v4: 15-90088405-T-G
• MyVariant Identifiers: chr15:g.90631637T>G (hg19) ; chr15:g.90088405T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088405T>G , CM000677.2:g.90088405T>G	GRCh38
NC_000015.9:g.90631637T>G , CM000677.1:g.90631637T>G	GRCh37
NC_000015.8:g.88432641T>G	NCBI36
NG_023302.1:g.19072A>C , LRG_611:g.19072A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.632A>C MANE Select	ENSP00000331897.4:p.Asn211Thr
ENST00000330062.7:c.632A>C	ENSP00000331897.3:p.Asn211Thr
ENST00000540499.2:c.476A>C	ENSP00000446147.2:p.Asn159Thr
ENST00000559482.5:c.305A>C	ENSP00000453016.1:p.Asn102Thr
ENST00000560061.1:c.*257A>C	ENSP00000453254.1:n.*257A>C
NM_001289910.1:c.476A>C , LRG_611t1:c.476A>C	NP_001276839.1:p.Asn159Thr
NM_001290114.1:c.242A>C	NP_001277043.1:p.Asn81Thr
NM_002168.3:c.632A>C , LRG_611t2:c.632A>C	NP_002159.2:p.Asn211Thr
NM_001290114.2:c.242A>C	NP_001277043.1:p.Asn81Thr
NM_002168.4:c.632A>C MANE Select	NP_002159.2:p.Asn211Thr