Canonical Allele Identifier: CA358027234
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320744A>C , CM000666.2:g.119320744A>C GRCh38
NC_000004.11:g.120241899A>C , CM000666.1:g.120241899A>C GRCh37
NC_000004.10:g.120461347A>C NCBI36
NG_011444.1:g.6418T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.166T>G MANE Select ENSP00000274024.3:p.Phe56Val
ENST00000274024.3:c.166T>G ENSP00000274024.3:p.Phe56Val
NM_000134.3:c.166T>G NP_000125.2:p.Phe56Val
NM_000134.4:c.166T>G MANE Select NP_000125.2:p.Phe56Val