Canonical Allele Identifier: CA1797411960
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1585810441
gnomAD v4: 8-81478463-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478463C>T , CM000670.2:g.81478463C>T GRCh38
NC_000008.10:g.82390698C>T , CM000670.1:g.82390698C>T GRCh37
NC_000008.9:g.82553253C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*402G>A MANE Select ENSP00000256104.4:n.*402G>A
ENST00000256104.4:c.*402G>A ENSP00000256104.4:n.*402G>A
XR_001745980.1:n.514+16489C>T
NM_001442.3:c.*402G>A MANE Select NP_001433.1:n.*402G>A
Search 100 bp 5'
Search 100 bp 3'