Canonical Allele Identifier: CA2687741558
Gene: FABP4 HGNC NCBI

Linked Data

gnomAD v4: 8-81478553-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478553C>T , CM000670.2:g.81478553C>T GRCh38
NC_000008.10:g.82390788C>T , CM000670.1:g.82390788C>T GRCh37
NC_000008.9:g.82553343C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*312G>A MANE Select ENSP00000256104.4:n.*312G>A
ENST00000256104.4:c.*312G>A ENSP00000256104.4:n.*312G>A
NM_001442.2:c.*312G>A NP_001433.1:n.*312G>A
XR_001745980.1:n.514+16579C>T
NM_001442.3:c.*312G>A MANE Select NP_001433.1:n.*312G>A
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