Canonical Allele Identifier: CA1488878555
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320782T= , CM000666.2:g.119320782T= GRCh38
NC_000004.11:g.120241937T= , CM000666.1:g.120241937T= GRCh37
NC_000004.10:g.120461385T= NCBI36
NG_011444.1:g.6380A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.128A= MANE Select ENSP00000274024.3:p.Gln43=
ENST00000274024.3:c.128A= ENSP00000274024.3:p.Gln43=
NM_000134.3:c.128A= NP_000125.2:p.Gln43=
NM_000134.4:c.128A= MANE Select NP_000125.2:p.Gln43=