Canonical Allele Identifier: CA554157164
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1398699852

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320659A>G , CM000666.2:g.119320659A>G GRCh38
NC_000004.11:g.120241814A>G , CM000666.1:g.120241814A>G GRCh37
NC_000004.10:g.120461262A>G NCBI36
NG_011444.1:g.6503T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+11T>C MANE Select ENSP00000274024.3:n.240+11T>C
ENST00000274024.3:c.240+11T>C ENSP00000274024.3:n.240+11T>C
NM_000134.3:c.240+11T>C NP_000125.2:n.240+11T>C
NM_000134.4:c.240+11T>C MANE Select NP_000125.2:n.240+11T>C