Canonical Allele Identifier: CA1048502728
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1700185680
gnomAD v3: 3-59705928-A-G
gnomAD v4: 3-59705928-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705928A>G , CM000665.2:g.59705928A>G GRCh38
NC_000003.11:g.59691654A>G , CM000665.1:g.59691654A>G GRCh37
NC_000003.10:g.59666694A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002959675.1:n.1218-103804A>G