Canonical Allele Identifier: CA440890628
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241870A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320715A>G , CM000666.2:g.119320715A>G GRCh38
NC_000004.11:g.120241870A>G , CM000666.1:g.120241870A>G GRCh37
NC_000004.10:g.120461318A>G NCBI36
NG_011444.1:g.6447T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.195T>C MANE Select ENSP00000274024.3:p.Leu65=
ENST00000274024.3:c.195T>C ENSP00000274024.3:p.Leu65=
NM_000134.3:c.195T>C NP_000125.2:p.Leu65=
NM_000134.4:c.195T>C MANE Select NP_000125.2:p.Leu65=
Search 100 bp 5'
Search 100 bp 3'