Canonical Allele Identifier: CA305861774
Gene: CYP4F3 HGNC NCBI

Linked Data

dbSNP Id: rs897489654
gnomAD v3: 19-15640691-G-A
gnomAD v4: 19-15640691-G-A
MyVariant Identifiers: chr19:g.15640691G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15640691G>A , CM000681.2:g.15640691G>A GRCh38
NC_000019.9:g.15751501G>A , CM000681.1:g.15751501G>A GRCh37
NC_000019.8:g.15612501G>A NCBI36
NG_007964.1:g.4795G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000620621.4:c.344-6361G>A ENSP00000478605.1:n.344-6361G>A
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