Canonical Allele Identifier: CA1048502716
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1700184788
gnomAD v3: 3-59705849-G-A
gnomAD v4: 3-59705849-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705849G>A , CM000665.2:g.59705849G>A GRCh38
NC_000003.11:g.59691575G>A , CM000665.1:g.59691575G>A GRCh37
NC_000003.10:g.59666615G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103883G>A