Canonical Allele Identifier: CA2687741735
Gene: FABP4 HGNC NCBI

Linked Data

gnomAD v4: 8-81478770-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478770A>T , CM000670.2:g.81478770A>T GRCh38
NC_000008.10:g.82391005A>T , CM000670.1:g.82391005A>T GRCh37
NC_000008.9:g.82553560A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*95T>A MANE Select ENSP00000256104.4:n.*95T>A
ENST00000256104.4:c.*95T>A ENSP00000256104.4:n.*95T>A
ENST00000518669.5:n.429T>A
ENST00000521734.1:n.703T>A
ENST00000522659.1:c.*370T>A ENSP00000428385.1:n.*370T>A
NM_001442.2:c.*95T>A NP_001433.1:n.*95T>A
XR_001745980.1:n.514+16796A>T
NM_001442.3:c.*95T>A MANE Select NP_001433.1:n.*95T>A