Canonical Allele Identifier: CA180381968
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs983438419
gnomAD v2: 8-82391003-T-G
gnomAD v3: 8-81478768-T-G
gnomAD v4: 8-81478768-T-G
MyVariant Identifiers: chr8:g.82391003T>G (hg19) chr8:g.81478768T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478768T>G , CM000670.2:g.81478768T>G GRCh38
NC_000008.10:g.82391003T>G , CM000670.1:g.82391003T>G GRCh37
NC_000008.9:g.82553558T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*97A>C MANE Select ENSP00000256104.4:n.*97A>C
ENST00000256104.4:c.*97A>C ENSP00000256104.4:n.*97A>C
ENST00000518669.5:n.431A>C
ENST00000521734.1:n.705A>C
ENST00000522659.1:c.*372A>C ENSP00000428385.1:n.*372A>C
NM_001442.2:c.*97A>C NP_001433.1:n.*97A>C
XR_001745980.1:n.514+16794T>G
NM_001442.3:c.*97A>C MANE Select NP_001433.1:n.*97A>C
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