Canonical Allele Identifier: CA3059786
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1553986133

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320758T>C , CM000666.2:g.119320758T>C GRCh38
NC_000004.11:g.120241913T>C , CM000666.1:g.120241913T>C GRCh37
NC_000004.10:g.120461361T>C NCBI36
NG_011444.1:g.6404A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.152A>G MANE Select ENSP00000274024.3:p.Lys51Arg
ENST00000274024.3:c.152A>G ENSP00000274024.3:p.Lys51Arg
NM_000134.3:c.152A>G NP_000125.2:p.Lys51Arg
NM_000134.4:c.152A>G MANE Select NP_000125.2:p.Lys51Arg