Canonical Allele Identifier: CA440890772
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241894T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320739T>C , CM000666.2:g.119320739T>C GRCh38
NC_000004.11:g.120241894T>C , CM000666.1:g.120241894T>C GRCh37
NC_000004.10:g.120461342T>C NCBI36
NG_011444.1:g.6423A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.171A>G MANE Select ENSP00000274024.3:p.Arg57=
ENST00000274024.3:c.171A>G ENSP00000274024.3:p.Arg57=
NM_000134.3:c.171A>G NP_000125.2:p.Arg57=
NM_000134.4:c.171A>G MANE Select NP_000125.2:p.Arg57=
Search 100 bp 5'
Search 100 bp 3'