Canonical Allele Identifier: CA180381906
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs929881047
gnomAD v2: 8-82390763-C-A
gnomAD v3: 8-81478528-C-A
gnomAD v4: 8-81478528-C-A
MyVariant Identifiers: chr8:g.82390763C>A (hg19) chr8:g.81478528C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478528C>A , CM000670.2:g.81478528C>A GRCh38
NC_000008.10:g.82390763C>A , CM000670.1:g.82390763C>A GRCh37
NC_000008.9:g.82553318C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*337G>T MANE Select ENSP00000256104.4:n.*337G>T
ENST00000256104.4:c.*337G>T ENSP00000256104.4:n.*337G>T
NM_001442.2:c.*337G>T NP_001433.1:n.*337G>T
XR_001745980.1:n.514+16554C>A
NM_001442.3:c.*337G>T MANE Select NP_001433.1:n.*337G>T
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