Canonical Allele Identifier: CA908843456
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs184341171
gnomAD v3: 3-59705805-G-A
gnomAD v4: 3-59705805-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705805G>A , CM000665.2:g.59705805G>A GRCh38
NC_000003.11:g.59691531G>A , CM000665.1:g.59691531G>A GRCh37
NC_000003.10:g.59666571G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103927G>A