Canonical Allele Identifier: CA358027456
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320774T>G , CM000666.2:g.119320774T>G GRCh38
NC_000004.11:g.120241929T>G , CM000666.1:g.120241929T>G GRCh37
NC_000004.10:g.120461377T>G NCBI36
NG_011444.1:g.6388A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.136A>C MANE Select ENSP00000274024.3:p.Asn46His
ENST00000274024.3:c.136A>C ENSP00000274024.3:p.Asn46His
NM_000134.3:c.136A>C NP_000125.2:p.Asn46His
NM_000134.4:c.136A>C MANE Select NP_000125.2:p.Asn46His