Canonical Allele Identifier: CA855860572
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1432183403
MyVariant Identifiers: chr8:g.82390899A>C (hg19) chr8:g.81478664A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478664A>C , CM000670.2:g.81478664A>C GRCh38
NC_000008.10:g.82390899A>C , CM000670.1:g.82390899A>C GRCh37
NC_000008.9:g.82553454A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*201T>G MANE Select ENSP00000256104.4:n.*201T>G
ENST00000256104.4:c.*201T>G ENSP00000256104.4:n.*201T>G
NM_001442.2:c.*201T>G NP_001433.1:n.*201T>G
XR_001745980.1:n.514+16690A>C
NM_001442.3:c.*201T>G MANE Select NP_001433.1:n.*201T>G
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