Canonical Allele Identifier: CA180381917
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs999925252
gnomAD v3: 8-81478548-A-G
gnomAD v4: 8-81478548-A-G
MyVariant Identifiers: chr8:g.82390783A>G (hg19) chr8:g.81478548A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478548A>G , CM000670.2:g.81478548A>G GRCh38
NC_000008.10:g.82390783A>G , CM000670.1:g.82390783A>G GRCh37
NC_000008.9:g.82553338A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*317T>C MANE Select ENSP00000256104.4:n.*317T>C
ENST00000256104.4:c.*317T>C ENSP00000256104.4:n.*317T>C
NM_001442.2:c.*317T>C NP_001433.1:n.*317T>C
XR_001745980.1:n.514+16574A>G
NM_001442.3:c.*317T>C MANE Select NP_001433.1:n.*317T>C
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