Canonical Allele Identifier: CA1488878468
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320568G= , CM000666.2:g.119320568G= GRCh38
NC_000004.11:g.120241723G= , CM000666.1:g.120241723G= GRCh37
NC_000004.10:g.120461171G= NCBI36
NG_011444.1:g.6594C=

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+102C= MANE Select ENSP00000274024.3:n.240+102C=
ENST00000274024.3:c.240+102C= ENSP00000274024.3:n.240+102C=
NM_000134.3:c.240+102C= NP_000125.2:n.240+102C=
NM_000134.4:c.240+102C= MANE Select NP_000125.2:n.240+102C=