Canonical Allele Identifier: CA440891161
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241948C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320793C>T , CM000666.2:g.119320793C>T GRCh38
NC_000004.11:g.120241948C>T , CM000666.1:g.120241948C>T GRCh37
NC_000004.10:g.120461396C>T NCBI36
NG_011444.1:g.6369G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.117G>A MANE Select ENSP00000274024.3:p.Leu39=
ENST00000274024.3:c.117G>A ENSP00000274024.3:p.Leu39=
NM_000134.3:c.117G>A NP_000125.2:p.Leu39=
NM_000134.4:c.117G>A MANE Select NP_000125.2:p.Leu39=
Search 100 bp 5'
Search 100 bp 3'