Canonical Allele Identifier: CA104693449
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs867211181
MyVariant Identifiers: chr4:g.120241888A>T (hg19) chr4:g.119320733A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320733A>T , CM000666.2:g.119320733A>T GRCh38
NC_000004.11:g.120241888A>T , CM000666.1:g.120241888A>T GRCh37
NC_000004.10:g.120461336A>T NCBI36
NG_011444.1:g.6429T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.177T>A MANE Select ENSP00000274024.3:p.Ile59=
ENST00000274024.3:c.177T>A ENSP00000274024.3:p.Ile59=
NM_000134.3:c.177T>A NP_000125.2:p.Ile59=
NM_000134.4:c.177T>A MANE Select NP_000125.2:p.Ile59=
Search 100 bp 5'
Search 100 bp 3'