Canonical Allele Identifier: CA1488878509
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320666T= , CM000666.2:g.119320666T= GRCh38
NC_000004.11:g.120241821T= , CM000666.1:g.120241821T= GRCh37
NC_000004.10:g.120461269T= NCBI36
NG_011444.1:g.6496A=

Transcript Alleles

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