Canonical Allele Identifier: CA1488878466
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320560G= , CM000666.2:g.119320560G= GRCh38
NC_000004.11:g.120241715G= , CM000666.1:g.120241715G= GRCh37
NC_000004.10:g.120461163G= NCBI36
NG_011444.1:g.6602C=

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+110C= MANE Select ENSP00000274024.3:n.240+110C=
ENST00000274024.3:c.240+110C= ENSP00000274024.3:n.240+110C=
NM_000134.3:c.240+110C= NP_000125.2:n.240+110C=
NM_000134.4:c.240+110C= MANE Select NP_000125.2:n.240+110C=