Canonical Allele Identifier: CA1048502792
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1700187050
gnomAD v3: 3-59706073-A-G
gnomAD v4: 3-59706073-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59706073A>G , CM000665.2:g.59706073A>G GRCh38
NC_000003.11:g.59691799A>G , CM000665.1:g.59691799A>G GRCh37
NC_000003.10:g.59666839A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103659A>G