Canonical Allele Identifier: CA1067271689
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs991475796
gnomAD v3: 4-119320587-A-T
gnomAD v4: 4-119320587-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320587A>T , CM000666.2:g.119320587A>T GRCh38
NC_000004.11:g.120241742A>T , CM000666.1:g.120241742A>T GRCh37
NC_000004.10:g.120461190A>T NCBI36
NG_011444.1:g.6575T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+83T>A MANE Select ENSP00000274024.3:n.240+83T>A
ENST00000274024.3:c.240+83T>A ENSP00000274024.3:n.240+83T>A
NM_000134.3:c.240+83T>A NP_000125.2:n.240+83T>A
NM_000134.4:c.240+83T>A MANE Select NP_000125.2:n.240+83T>A
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