Canonical Allele Identifier: CA358026712
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320680G>T , CM000666.2:g.119320680G>T GRCh38
NC_000004.11:g.120241835G>T , CM000666.1:g.120241835G>T GRCh37
NC_000004.10:g.120461283G>T NCBI36
NG_011444.1:g.6482C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.230C>A MANE Select ENSP00000274024.3:p.Thr77Asn
ENST00000274024.3:c.230C>A ENSP00000274024.3:p.Thr77Asn
NM_000134.3:c.230C>A NP_000125.2:p.Thr77Asn
NM_000134.4:c.230C>A MANE Select NP_000125.2:p.Thr77Asn