Canonical Allele Identifier: CA2671895130
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320850del , CM000666.2:g.119320850del GRCh38
NC_000004.11:g.120242005del , CM000666.1:g.120242005del GRCh37
NC_000004.10:g.120461453del NCBI36
NG_011444.1:g.6315del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.68-5del MANE Select ENSP00000274024.3:n.68-5del
ENST00000274024.3:c.68-5del ENSP00000274024.3:n.68-5del
NM_000134.3:c.68-5del NP_000125.2:n.68-5del
NM_000134.4:c.68-5del MANE Select NP_000125.2:n.68-5del