Canonical Allele Identifier: CA1488878518
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320685G= , CM000666.2:g.119320685G= GRCh38
NC_000004.11:g.120241840G= , CM000666.1:g.120241840G= GRCh37
NC_000004.10:g.120461288G= NCBI36
NG_011444.1:g.6477C=

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.225C= MANE Select ENSP00000274024.3:p.Asp75=
ENST00000274024.3:c.225C= ENSP00000274024.3:p.Asp75=
NM_000134.3:c.225C= NP_000125.2:p.Asp75=
NM_000134.4:c.225C= MANE Select NP_000125.2:p.Asp75=