Canonical Allele Identifier: CA855860601
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1486530363
gnomAD v3: 8-81478707-T-A
gnomAD v4: 8-81478707-T-A
MyVariant Identifiers: chr8:g.82390942T>A (hg19) chr8:g.81478707T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478707T>A , CM000670.2:g.81478707T>A GRCh38
NC_000008.10:g.82390942T>A , CM000670.1:g.82390942T>A GRCh37
NC_000008.9:g.82553497T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*158A>T MANE Select ENSP00000256104.4:n.*158A>T
ENST00000256104.4:c.*158A>T ENSP00000256104.4:n.*158A>T
ENST00000518669.5:n.492A>T
ENST00000522659.1:c.*433A>T ENSP00000428385.1:n.*433A>T
NM_001442.2:c.*158A>T NP_001433.1:n.*158A>T
XR_001745980.1:n.514+16733T>A
NM_001442.3:c.*158A>T MANE Select NP_001433.1:n.*158A>T
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