Canonical Allele Identifier: CA783658252
Gene: CYP4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1303884927
gnomAD v3: 19-15640619-C-G
gnomAD v4: 19-15640619-C-G
MyVariant Identifiers: chr19:g.15751429C>G (hg19) chr19:g.15640619C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15640619C>G , CM000681.2:g.15640619C>G GRCh38
NC_000019.9:g.15751429C>G , CM000681.1:g.15751429C>G GRCh37
NC_000019.8:g.15612429C>G NCBI36
NG_007964.1:g.4723C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000620621.4:c.344-6433C>G ENSP00000478605.1:n.344-6433C>G
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