Canonical Allele Identifier: CA358027427
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320771T>G , CM000666.2:g.119320771T>G GRCh38
NC_000004.11:g.120241926T>G , CM000666.1:g.120241926T>G GRCh37
NC_000004.10:g.120461374T>G NCBI36
NG_011444.1:g.6391A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.139A>C MANE Select ENSP00000274024.3:p.Lys47Gln
ENST00000274024.3:c.139A>C ENSP00000274024.3:p.Lys47Gln
NM_000134.3:c.139A>C NP_000125.2:p.Lys47Gln
NM_000134.4:c.139A>C MANE Select NP_000125.2:p.Lys47Gln