Canonical Allele Identifier: CA358027022
Gene: FABP2 HGNC NCBI

Linked Data

gnomAD v4: 4-119320717-G-T
MyVariant Identifiers: chr4:g.120241872G>T (hg19) chr4:g.119320717G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320717G>T , CM000666.2:g.119320717G>T GRCh38
NC_000004.11:g.120241872G>T , CM000666.1:g.120241872G>T GRCh37
NC_000004.10:g.120461320G>T NCBI36
NG_011444.1:g.6445C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.193C>A MANE Select ENSP00000274024.3:p.Leu65Ile
ENST00000274024.3:c.193C>A ENSP00000274024.3:p.Leu65Ile
NM_000134.3:c.193C>A NP_000125.2:p.Leu65Ile
NM_000134.4:c.193C>A MANE Select NP_000125.2:p.Leu65Ile
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