Canonical Allele Identifier: CA358027384
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241922A>T (hg19) chr4:g.119320767A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320767A>T , CM000666.2:g.119320767A>T GRCh38
NC_000004.11:g.120241922A>T , CM000666.1:g.120241922A>T GRCh37
NC_000004.10:g.120461370A>T NCBI36
NG_011444.1:g.6395T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.143T>A MANE Select ENSP00000274024.3:p.Phe48Tyr
ENST00000274024.3:c.143T>A ENSP00000274024.3:p.Phe48Tyr
NM_000134.3:c.143T>A NP_000125.2:p.Phe48Tyr
NM_000134.4:c.143T>A MANE Select NP_000125.2:p.Phe48Tyr
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