Canonical Allele Identifier: CA1488878519
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320687C= , CM000666.2:g.119320687C= GRCh38
NC_000004.11:g.120241842C= , CM000666.1:g.120241842C= GRCh37
NC_000004.10:g.120461290C= NCBI36
NG_011444.1:g.6475G=

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.223G= MANE Select ENSP00000274024.3:p.Asp75=
ENST00000274024.3:c.223G= ENSP00000274024.3:p.Asp75=
NM_000134.3:c.223G= NP_000125.2:p.Asp75=
NM_000134.4:c.223G= MANE Select NP_000125.2:p.Asp75=