Canonical Allele Identifier: CA1797412209
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1808010028
gnomAD v4: 8-81478738-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478738A>T , CM000670.2:g.81478738A>T GRCh38
NC_000008.10:g.82390973A>T , CM000670.1:g.82390973A>T GRCh37
NC_000008.9:g.82553528A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*127T>A MANE Select ENSP00000256104.4:n.*127T>A
ENST00000256104.4:c.*127T>A ENSP00000256104.4:n.*127T>A
ENST00000518669.5:n.461T>A
ENST00000521734.1:n.735T>A
ENST00000522659.1:c.*402T>A ENSP00000428385.1:n.*402T>A
NM_001442.2:c.*127T>A NP_001433.1:n.*127T>A
XR_001745980.1:n.514+16764A>T
NM_001442.3:c.*127T>A MANE Select NP_001433.1:n.*127T>A