Canonical Allele Identifier: CA1488878545
Gene: FABP2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.154G= MANE Select ENSP00000274024.3:p.Glu52=
ENST00000274024.3:c.154G= ENSP00000274024.3:p.Glu52=
NM_000134.3:c.154G= NP_000125.2:p.Glu52=
NM_000134.4:c.154G= MANE Select NP_000125.2:p.Glu52=