Canonical Allele Identifier: CA14707115
Gene: CYP4F23P HGNC NCBI

Linked Data

dbSNP Id: rs1273516
gnomAD v2: 19-15677710-G-A
gnomAD v3: 19-15566899-G-A
gnomAD v4: 19-15566899-G-A
MyVariant Identifiers: chr19:g.15677710G>A (hg19) chr19:g.15566899G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15566899G>A , CM000681.2:g.15566899G>A GRCh38
NC_000019.9:g.15677710G>A , CM000681.1:g.15677710G>A GRCh37
NC_000019.8:g.15538710G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000593402.6:n.201+2625G>A
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