Canonical Allele Identifier: CA180381940
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs906748910
MyVariant Identifiers: chr8:g.82390898C>T (hg19) chr8:g.81478663C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478663C>T , CM000670.2:g.81478663C>T GRCh38
NC_000008.10:g.82390898C>T , CM000670.1:g.82390898C>T GRCh37
NC_000008.9:g.82553453C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*202G>A MANE Select ENSP00000256104.4:n.*202G>A
ENST00000256104.4:c.*202G>A ENSP00000256104.4:n.*202G>A
NM_001442.2:c.*202G>A NP_001433.1:n.*202G>A
XR_001745980.1:n.514+16689C>T
NM_001442.3:c.*202G>A MANE Select NP_001433.1:n.*202G>A
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