Canonical Allele Identifier: CA2687741572
Gene: FABP4 HGNC NCBI

Linked Data

gnomAD v4: 8-81478574-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478574T>C , CM000670.2:g.81478574T>C GRCh38
NC_000008.10:g.82390809T>C , CM000670.1:g.82390809T>C GRCh37
NC_000008.9:g.82553364T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*291A>G MANE Select ENSP00000256104.4:n.*291A>G
ENST00000256104.4:c.*291A>G ENSP00000256104.4:n.*291A>G
NM_001442.2:c.*291A>G NP_001433.1:n.*291A>G
XR_001745980.1:n.514+16600T>C
NM_001442.3:c.*291A>G MANE Select NP_001433.1:n.*291A>G