Canonical Allele Identifier: CA1488878488
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320611A= , CM000666.2:g.119320611A= GRCh38
NC_000004.11:g.120241766A= , CM000666.1:g.120241766A= GRCh37
NC_000004.10:g.120461214A= NCBI36
NG_011444.1:g.6551T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.240+59T= MANE Select ENSP00000274024.3:n.240+59T=
ENST00000274024.3:c.240+59T= ENSP00000274024.3:n.240+59T=
NM_000134.3:c.240+59T= NP_000125.2:n.240+59T=
NM_000134.4:c.240+59T= MANE Select NP_000125.2:n.240+59T=