Canonical Allele Identifier: CA1488878441
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1755648292

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320508del , CM000666.2:g.119320508del GRCh38
NC_000004.11:g.120241663del , CM000666.1:g.120241663del GRCh37
NC_000004.10:g.120461111del NCBI36
NG_011444.1:g.6654del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.240+162del MANE Select ENSP00000274024.3:n.240+162del
ENST00000274024.3:c.240+162del ENSP00000274024.3:n.240+162del
NM_000134.3:c.240+162del NP_000125.2:n.240+162del
NM_000134.4:c.240+162del MANE Select NP_000125.2:n.240+162del