Canonical Allele Identifier: CA180381946
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs559655366
gnomAD v2: 8-82390934-A-C
gnomAD v3: 8-81478699-A-C
gnomAD v4: 8-81478699-A-C
MyVariant Identifiers: chr8:g.82390934A>C (hg19) chr8:g.81478699A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478699A>C , CM000670.2:g.81478699A>C GRCh38
NC_000008.10:g.82390934A>C , CM000670.1:g.82390934A>C GRCh37
NC_000008.9:g.82553489A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*166T>G MANE Select ENSP00000256104.4:n.*166T>G
ENST00000256104.4:c.*166T>G ENSP00000256104.4:n.*166T>G
ENST00000518669.5:n.500T>G
ENST00000522659.1:c.*441T>G ENSP00000428385.1:n.*441T>G
NM_001442.2:c.*166T>G NP_001433.1:n.*166T>G
XR_001745980.1:n.514+16725A>C
NM_001442.3:c.*166T>G MANE Select NP_001433.1:n.*166T>G
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