Canonical Allele Identifier: CA908843508
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1392050644
gnomAD v3: 3-59705908-T-A
gnomAD v4: 3-59705908-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705908T>A , CM000665.2:g.59705908T>A GRCh38
NC_000003.11:g.59691634T>A , CM000665.1:g.59691634T>A GRCh37
NC_000003.10:g.59666674T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002959675.1:n.1218-103824T>A