Canonical Allele Identifier: CA855860653
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1303744832
gnomAD v3: 8-81478770-A-C
gnomAD v4: 8-81478770-A-C
MyVariant Identifiers: chr8:g.82391005A>C (hg19) chr8:g.81478770A>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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