Canonical Allele Identifier: CA2671895124
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320755del , CM000666.2:g.119320755del GRCh38
NC_000004.11:g.120241910del , CM000666.1:g.120241910del GRCh37
NC_000004.10:g.120461358del NCBI36
NG_011444.1:g.6408del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.156del MANE Select ENSP00000274024.3:p.Glu52AspfsTer22
ENST00000274024.3:c.156del ENSP00000274024.3:p.Glu52AspfsTer22
NM_000134.3:c.156del NP_000125.2:p.Glu52AspfsTer22
NM_000134.4:c.156del MANE Select NP_000125.2:p.Glu52AspfsTer22