Canonical Allele Identifier: CA855860646

Gene: FABP4

Linked Data

• dbSNP Id: rs1398621468
• MyVariant Identifiers: chr8:g.82390995T>A (hg19) ; chr8:g.81478760T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.81478760T>A , CM000670.2:g.81478760T>A	GRCh38
NC_000008.10:g.82390995T>A , CM000670.1:g.82390995T>A	GRCh37
NC_000008.9:g.82553550T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256104.5:c.*105A>T MANE Select	ENSP00000256104.4:n.*105A>T
ENST00000256104.4:c.*105A>T	ENSP00000256104.4:n.*105A>T
ENST00000518669.5:n.439A>T
ENST00000521734.1:n.713A>T
ENST00000522659.1:c.*380A>T	ENSP00000428385.1:n.*380A>T
NM_001442.2:c.*105A>T	NP_001433.1:n.*105A>T
XR_001745980.1:n.514+16786T>A
NM_001442.3:c.*105A>T MANE Select	NP_001433.1:n.*105A>T