Canonical Allele Identifier: CA2671895125
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320756del , CM000666.2:g.119320756del GRCh38
NC_000004.11:g.120241911del , CM000666.1:g.120241911del GRCh37
NC_000004.10:g.120461359del NCBI36
NG_011444.1:g.6406del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.154del MANE Select ENSP00000274024.3:p.Glu52AsnfsTer22
ENST00000274024.3:c.154del ENSP00000274024.3:p.Glu52AsnfsTer22
NM_000134.3:c.154del NP_000125.2:p.Glu52AsnfsTer22
NM_000134.4:c.154del MANE Select NP_000125.2:p.Glu52AsnfsTer22