Canonical Allele Identifier: CA1115843854
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1398621468
gnomAD v3: 8-81478760-T-C
gnomAD v4: 8-81478760-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478760T>C , CM000670.2:g.81478760T>C GRCh38
NC_000008.10:g.82390995T>C , CM000670.1:g.82390995T>C GRCh37
NC_000008.9:g.82553550T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*105A>G MANE Select ENSP00000256104.4:n.*105A>G
ENST00000256104.4:c.*105A>G ENSP00000256104.4:n.*105A>G
ENST00000518669.5:n.439A>G
ENST00000521734.1:n.713A>G
ENST00000522659.1:c.*380A>G ENSP00000428385.1:n.*380A>G
NM_001442.2:c.*105A>G NP_001433.1:n.*105A>G
XR_001745980.1:n.514+16786T>C
NM_001442.3:c.*105A>G MANE Select NP_001433.1:n.*105A>G
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