Canonical Allele Identifier: CA3059763
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs779976025

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320648T>G , CM000666.2:g.119320648T>G GRCh38
NC_000004.11:g.120241803T>G , CM000666.1:g.120241803T>G GRCh37
NC_000004.10:g.120461251T>G NCBI36
NG_011444.1:g.6514A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+22A>C MANE Select ENSP00000274024.3:n.240+22A>C
ENST00000274024.3:c.240+22A>C ENSP00000274024.3:n.240+22A>C
NM_000134.3:c.240+22A>C NP_000125.2:n.240+22A>C
NM_000134.4:c.240+22A>C MANE Select NP_000125.2:n.240+22A>C