Canonical Allele Identifier: CA75934131
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs371851737
gnomAD v2: 3-59691224-C-A
gnomAD v3: 3-59705498-C-A
gnomAD v4: 3-59705498-C-A
MyVariant Identifiers: chr3:g.59691224C>A (hg19) chr3:g.59705498C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705498C>A , CM000665.2:g.59705498C>A GRCh38
NC_000003.11:g.59691224C>A , CM000665.1:g.59691224C>A GRCh37
NC_000003.10:g.59666264C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-104234C>A
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