Canonical Allele Identifier: CA1048502619
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1700181379
gnomAD v3: 3-59705516-C-A
gnomAD v4: 3-59705516-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705516C>A , CM000665.2:g.59705516C>A GRCh38
NC_000003.11:g.59691242C>A , CM000665.1:g.59691242C>A GRCh37
NC_000003.10:g.59666282C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-104216C>A
Search 100 bp 5'
Search 100 bp 3'