Canonical Allele Identifier: CA305861758
Gene: CYP4F3 HGNC NCBI

Linked Data

dbSNP Id: rs889351612
gnomAD v2: 19-15751463-T-C
gnomAD v3: 19-15640653-T-C
gnomAD v4: 19-15640653-T-C
MyVariant Identifiers: chr19:g.15751463T>C (hg19) chr19:g.15640653T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15640653T>C , CM000681.2:g.15640653T>C GRCh38
NC_000019.9:g.15751463T>C , CM000681.1:g.15751463T>C GRCh37
NC_000019.8:g.15612463T>C NCBI36
NG_007964.1:g.4757T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000620621.4:c.344-6399T>C ENSP00000478605.1:n.344-6399T>C
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