Canonical Allele Identifier: CA1048502779
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1343847354
gnomAD v3: 3-59706034-C-A
gnomAD v4: 3-59706034-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59706034C>A , CM000665.2:g.59706034C>A GRCh38
NC_000003.11:g.59691760C>A , CM000665.1:g.59691760C>A GRCh37
NC_000003.10:g.59666800C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002959675.1:n.1218-103698C>A