Canonical Allele Identifier: CA3059785

Gene: FABP2

Linked Data

• dbSNP Id: rs770616869
• ExAC: 4:120241911 CT / C
• gnomAD v2: 4-120241911-CT-C
• gnomAD v3: 4-119320756-CT-C
• gnomAD v4: 4-119320756-CT-C
• MyVariant Identifiers: chr4:g.120241912del (hg19) ; chr4:g.119320757del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320759del , CM000666.2:g.119320759del	GRCh38
NC_000004.11:g.120241914del , CM000666.1:g.120241914del	GRCh37
NC_000004.10:g.120461362del	NCBI36
NG_011444.1:g.6405del

Transcript Alleles

HGVS	Amino-acid change
ENST00000274024.4:c.153del MANE Select	ENSP00000274024.3:p.Glu52AsnfsTer22
ENST00000274024.3:c.153del	ENSP00000274024.3:p.Glu52AsnfsTer22
NM_000134.3:c.153del	NP_000125.2:p.Glu52AsnfsTer22
NM_000134.4:c.153del MANE Select	NP_000125.2:p.Glu52AsnfsTer22