Canonical Allele Identifier: CA180381951
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs181258114
gnomAD v2: 8-82390939-A-T
gnomAD v3: 8-81478704-A-T
gnomAD v4: 8-81478704-A-T
MyVariant Identifiers: chr8:g.82390939A>T (hg19) chr8:g.81478704A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478704A>T , CM000670.2:g.81478704A>T GRCh38
NC_000008.10:g.82390939A>T , CM000670.1:g.82390939A>T GRCh37
NC_000008.9:g.82553494A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*161T>A MANE Select ENSP00000256104.4:n.*161T>A
ENST00000256104.4:c.*161T>A ENSP00000256104.4:n.*161T>A
ENST00000518669.5:n.495T>A
ENST00000522659.1:c.*436T>A ENSP00000428385.1:n.*436T>A
NM_001442.2:c.*161T>A NP_001433.1:n.*161T>A
XR_001745980.1:n.514+16730A>T
NM_001442.3:c.*161T>A MANE Select NP_001433.1:n.*161T>A
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