Canonical Allele Identifier: CA1797412153
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1808008599
gnomAD v4: 8-81478677-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478677C>T , CM000670.2:g.81478677C>T GRCh38
NC_000008.10:g.82390912C>T , CM000670.1:g.82390912C>T GRCh37
NC_000008.9:g.82553467C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*188G>A MANE Select ENSP00000256104.4:n.*188G>A
ENST00000256104.4:c.*188G>A ENSP00000256104.4:n.*188G>A
NM_001442.2:c.*188G>A NP_001433.1:n.*188G>A
XR_001745980.1:n.514+16703C>T
NM_001442.3:c.*188G>A MANE Select NP_001433.1:n.*188G>A
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