Canonical Allele Identifier: CA3059779
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs776157369
ExAC: 4:120241851 T / A
gnomAD v2: 4-120241851-T-A
gnomAD v4: 4-119320696-T-A
MyVariant Identifiers: chr4:g.120241851T>A (hg19) chr4:g.119320696T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320696T>A , CM000666.2:g.119320696T>A GRCh38
NC_000004.11:g.120241851T>A , CM000666.1:g.120241851T>A GRCh37
NC_000004.10:g.120461299T>A NCBI36
NG_011444.1:g.6466A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.214A>T MANE Select ENSP00000274024.3:p.Asn72Tyr
ENST00000274024.3:c.214A>T ENSP00000274024.3:p.Asn72Tyr
NM_000134.3:c.214A>T NP_000125.2:p.Asn72Tyr
NM_000134.4:c.214A>T MANE Select NP_000125.2:p.Asn72Tyr
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