Canonical Allele Identifier: CA1488878536
Gene: FABP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320734A= , CM000666.2:g.119320734A= GRCh38
NC_000004.11:g.120241889A= , CM000666.1:g.120241889A= GRCh37
NC_000004.10:g.120461337A= NCBI36
NG_011444.1:g.6428T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.176T= MANE Select ENSP00000274024.3:p.Ile59=
ENST00000274024.3:c.176T= ENSP00000274024.3:p.Ile59=
NM_000134.3:c.176T= NP_000125.2:p.Ile59=
NM_000134.4:c.176T= MANE Select NP_000125.2:p.Ile59=
Search 100 bp 5'
Search 100 bp 3'