Canonical Allele Identifier: CA855860597
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1191316083
gnomAD v3: 8-81478705-AG-A
gnomAD v4: 8-81478705-AG-A
MyVariant Identifiers: chr8:g.82390941del (hg19) chr8:g.81478706del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478706del , CM000670.2:g.81478706del GRCh38
NC_000008.10:g.82390941del , CM000670.1:g.82390941del GRCh37
NC_000008.9:g.82553496del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*159del MANE Select ENSP00000256104.4:n.*159del
ENST00000256104.4:c.*159del ENSP00000256104.4:n.*159del
ENST00000518669.5:n.493del
ENST00000522659.1:c.*434del ENSP00000428385.1:n.*434del
NM_001442.2:c.*159del NP_001433.1:n.*159del
XR_001745980.1:n.514+16732del
NM_001442.3:c.*159del MANE Select NP_001433.1:n.*159del
Search 100 bp 5'
Search 100 bp 3'