Canonical Allele Identifier: CA180381922
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs372701687
gnomAD v2: 8-82390819-TA-T
gnomAD v3: 8-81478584-TA-T
gnomAD v4: 8-81478584-TA-T
MyVariant Identifiers: chr8:g.82390820del (hg19) chr8:g.81478585del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478585del , CM000670.2:g.81478585del GRCh38
NC_000008.10:g.82390820del , CM000670.1:g.82390820del GRCh37
NC_000008.9:g.82553375del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*280del MANE Select ENSP00000256104.4:n.*280del
ENST00000256104.4:c.*280del ENSP00000256104.4:n.*280del
NM_001442.2:c.*280del NP_001433.1:n.*280del
XR_001745980.1:n.514+16611del
NM_001442.3:c.*280del MANE Select NP_001433.1:n.*280del
Search 100 bp 5'
Search 100 bp 3'