Canonical Allele Identifier: CA3059801
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs769550240

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320839A>G , CM000666.2:g.119320839A>G GRCh38
NC_000004.11:g.120241994A>G , CM000666.1:g.120241994A>G GRCh37
NC_000004.10:g.120461442A>G NCBI36
NG_011444.1:g.6323T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.71T>C MANE Select ENSP00000274024.3:p.Val24Ala
ENST00000274024.3:c.71T>C ENSP00000274024.3:p.Val24Ala
NM_000134.3:c.71T>C NP_000125.2:p.Val24Ala
NM_000134.4:c.71T>C MANE Select NP_000125.2:p.Val24Ala