Canonical Allele Identifier: CA1488878573
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320824C= , CM000666.2:g.119320824C= GRCh38
NC_000004.11:g.120241979C= , CM000666.1:g.120241979C= GRCh37
NC_000004.10:g.120461427C= NCBI36
NG_011444.1:g.6338G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.86G= MANE Select ENSP00000274024.3:p.Arg29=
ENST00000274024.3:c.86G= ENSP00000274024.3:p.Arg29=
NM_000134.3:c.86G= NP_000125.2:p.Arg29=
NM_000134.4:c.86G= MANE Select NP_000125.2:p.Arg29=