Canonical Allele Identifier: CA1797411994
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1585810447
gnomAD v4: 8-81478502-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478502C>G , CM000670.2:g.81478502C>G GRCh38
NC_000008.10:g.82390737C>G , CM000670.1:g.82390737C>G GRCh37
NC_000008.9:g.82553292C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*363G>C MANE Select ENSP00000256104.4:n.*363G>C
ENST00000256104.4:c.*363G>C ENSP00000256104.4:n.*363G>C
NM_001442.2:c.*363G>C NP_001433.1:n.*363G>C
XR_001745980.1:n.514+16528C>G
NM_001442.3:c.*363G>C MANE Select NP_001433.1:n.*363G>C
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