Canonical Allele Identifier: CA1797412147
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1563527332
gnomAD v4: 8-81478667-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478667A>C , CM000670.2:g.81478667A>C GRCh38
NC_000008.10:g.82390902A>C , CM000670.1:g.82390902A>C GRCh37
NC_000008.9:g.82553457A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*198T>G MANE Select ENSP00000256104.4:n.*198T>G
ENST00000256104.4:c.*198T>G ENSP00000256104.4:n.*198T>G
NM_001442.2:c.*198T>G NP_001433.1:n.*198T>G
XR_001745980.1:n.514+16693A>C
NM_001442.3:c.*198T>G MANE Select NP_001433.1:n.*198T>G
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