Canonical Allele Identifier: CA1488878442
Gene: FABP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320519C= , CM000666.2:g.119320519C= GRCh38
NC_000004.11:g.120241674C= , CM000666.1:g.120241674C= GRCh37
NC_000004.10:g.120461122C= NCBI36
NG_011444.1:g.6643G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.240+151G= MANE Select ENSP00000274024.3:n.240+151G=
ENST00000274024.3:c.240+151G= ENSP00000274024.3:n.240+151G=
NM_000134.3:c.240+151G= NP_000125.2:n.240+151G=
NM_000134.4:c.240+151G= MANE Select NP_000125.2:n.240+151G=
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