Canonical Allele Identifier: CA1048502605
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1700180954
gnomAD v3: 3-59705473-G-A
gnomAD v4: 3-59705473-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705473G>A , CM000665.2:g.59705473G>A GRCh38
NC_000003.11:g.59691199G>A , CM000665.1:g.59691199G>A GRCh37
NC_000003.10:g.59666239G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-104259G>A