Canonical Allele Identifier: CA619547900

Gene: IDH2

Linked Data

• dbSNP Id: rs1230969813
• gnomAD v2: 15-90632026-CA-C
• gnomAD v3: 15-90088794-CA-C
• gnomAD v4: 15-90088794-CA-C
• MyVariant Identifiers: chr15:g.90632027del (hg19) ; chr15:g.90088795del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088796del , CM000677.2:g.90088796del	GRCh38
NC_000015.9:g.90632028del , CM000677.1:g.90632028del	GRCh37
NC_000015.8:g.88433032del	NCBI36
NG_023302.1:g.18682del , LRG_611:g.18682del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.374-48del MANE Select	ENSP00000331897.4:n.374-48del
ENST00000330062.7:c.374-48del	ENSP00000331897.3:n.374-48del
ENST00000540499.2:c.218-48del	ENSP00000446147.2:n.218-48del
ENST00000559482.5:c.208-293del	ENSP00000453016.1:n.208-293del
ENST00000560061.1:c.116-48del	ENSP00000453254.1:n.116-48del
NM_001289910.1:c.218-48del , LRG_611t1:c.218-48del	NP_001276839.1:n.218-48del
NM_001290114.1:c.-17-48del	NP_001277043.1:n.-17-48del
NM_002168.3:c.374-48del , LRG_611t2:c.374-48del	NP_002159.2:n.374-48del
NM_001290114.2:c.-17-48del	NP_001277043.1:n.-17-48del
NM_002168.4:c.374-48del MANE Select	NP_002159.2:n.374-48del