Canonical Allele Identifier: CA1488878435
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320493A= , CM000666.2:g.119320493A= GRCh38
NC_000004.11:g.120241648A= , CM000666.1:g.120241648A= GRCh37
NC_000004.10:g.120461096A= NCBI36
NG_011444.1:g.6669T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.240+177T= MANE Select ENSP00000274024.3:n.240+177T=
ENST00000274024.3:c.240+177T= ENSP00000274024.3:n.240+177T=
NM_000134.3:c.240+177T= NP_000125.2:n.240+177T=
NM_000134.4:c.240+177T= MANE Select NP_000125.2:n.240+177T=