Canonical Allele Identifier: CA358026984
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1755652963

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320713C>G , CM000666.2:g.119320713C>G GRCh38
NC_000004.11:g.120241868C>G , CM000666.1:g.120241868C>G GRCh37
NC_000004.10:g.120461316C>G NCBI36
NG_011444.1:g.6449G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.197G>C MANE Select ENSP00000274024.3:p.Gly66Ala
ENST00000274024.3:c.197G>C ENSP00000274024.3:p.Gly66Ala
NM_000134.3:c.197G>C NP_000125.2:p.Gly66Ala
NM_000134.4:c.197G>C MANE Select NP_000125.2:p.Gly66Ala