Canonical Allele Identifier: CA358026833
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs4834770

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320694A>T , CM000666.2:g.119320694A>T GRCh38
NC_000004.11:g.120241849A>T , CM000666.1:g.120241849A>T GRCh37
NC_000004.10:g.120461297A>T NCBI36
NG_011444.1:g.6468T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.216T>A MANE Select ENSP00000274024.3:p.Asn72Lys
ENST00000274024.3:c.216T>A ENSP00000274024.3:p.Asn72Lys
NM_000134.3:c.216T>A NP_000125.2:p.Asn72Lys
NM_000134.4:c.216T>A MANE Select NP_000125.2:p.Asn72Lys