Canonical Allele Identifier: CA1115843842
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1808009846
gnomAD v3: 8-81478731-T-C
gnomAD v4: 8-81478731-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478731T>C , CM000670.2:g.81478731T>C GRCh38
NC_000008.10:g.82390966T>C , CM000670.1:g.82390966T>C GRCh37
NC_000008.9:g.82553521T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*134A>G MANE Select ENSP00000256104.4:n.*134A>G
ENST00000256104.4:c.*134A>G ENSP00000256104.4:n.*134A>G
ENST00000518669.5:n.468A>G
ENST00000521734.1:n.742A>G
ENST00000522659.1:c.*409A>G ENSP00000428385.1:n.*409A>G
NM_001442.2:c.*134A>G NP_001433.1:n.*134A>G
XR_001745980.1:n.514+16757T>C
NM_001442.3:c.*134A>G MANE Select NP_001433.1:n.*134A>G