Canonical Allele Identifier: CA855860642
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1220522091
gnomAD v3: 8-81478739-A-T
gnomAD v4: 8-81478739-A-T
MyVariant Identifiers: chr8:g.82390974A>T (hg19) chr8:g.81478739A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478739A>T , CM000670.2:g.81478739A>T GRCh38
NC_000008.10:g.82390974A>T , CM000670.1:g.82390974A>T GRCh37
NC_000008.9:g.82553529A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*126T>A MANE Select ENSP00000256104.4:n.*126T>A
ENST00000256104.4:c.*126T>A ENSP00000256104.4:n.*126T>A
ENST00000518669.5:n.460T>A
ENST00000521734.1:n.734T>A
ENST00000522659.1:c.*401T>A ENSP00000428385.1:n.*401T>A
NM_001442.2:c.*126T>A NP_001433.1:n.*126T>A
XR_001745980.1:n.514+16765A>T
NM_001442.3:c.*126T>A MANE Select NP_001433.1:n.*126T>A
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