Canonical Allele Identifier: CA2687741701
Gene: FABP4 HGNC NCBI

Linked Data

gnomAD v4: 8-81478714-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478714A>T , CM000670.2:g.81478714A>T GRCh38
NC_000008.10:g.82390949A>T , CM000670.1:g.82390949A>T GRCh37
NC_000008.9:g.82553504A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*151T>A MANE Select ENSP00000256104.4:n.*151T>A
ENST00000256104.4:c.*151T>A ENSP00000256104.4:n.*151T>A
ENST00000518669.5:n.485T>A
ENST00000521734.1:n.759T>A
ENST00000522659.1:c.*426T>A ENSP00000428385.1:n.*426T>A
NM_001442.2:c.*151T>A NP_001433.1:n.*151T>A
XR_001745980.1:n.514+16740A>T
NM_001442.3:c.*151T>A MANE Select NP_001433.1:n.*151T>A