Canonical Allele Identifier: CA1797412168
Gene: FABP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478699A= , CM000670.2:g.81478699A= GRCh38
NC_000008.10:g.82390934A= , CM000670.1:g.82390934A= GRCh37
NC_000008.9:g.82553489A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*166T= MANE Select ENSP00000256104.4:n.*166T=
ENST00000256104.4:c.*166T= ENSP00000256104.4:n.*166T=
ENST00000518669.5:n.500T=
ENST00000522659.1:c.*441T= ENSP00000428385.1:n.*441T=
NM_001442.2:c.*166T= NP_001433.1:n.*166T=
XR_001745980.1:n.514+16725A=
NM_001442.3:c.*166T= MANE Select NP_001433.1:n.*166T=