Canonical Allele Identifier: CA3059782
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs376304732
ExAC: 4:120241889 A / G
gnomAD v2: 4-120241889-A-G
gnomAD v3: 4-119320734-A-G
gnomAD v4: 4-119320734-A-G
MyVariant Identifiers: chr4:g.120241889A>G (hg19) chr4:g.119320734A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320734A>G , CM000666.2:g.119320734A>G GRCh38
NC_000004.11:g.120241889A>G , CM000666.1:g.120241889A>G GRCh37
NC_000004.10:g.120461337A>G NCBI36
NG_011444.1:g.6428T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.176T>C MANE Select ENSP00000274024.3:p.Ile59Thr
ENST00000274024.3:c.176T>C ENSP00000274024.3:p.Ile59Thr
NM_000134.3:c.176T>C NP_000125.2:p.Ile59Thr
NM_000134.4:c.176T>C MANE Select NP_000125.2:p.Ile59Thr
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