Canonical Allele Identifier: CA543450386
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1314446039
gnomAD v2: 3-59691664-A-G
gnomAD v3: 3-59705938-A-G
gnomAD v4: 3-59705938-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705938A>G , CM000665.2:g.59705938A>G GRCh38
NC_000003.11:g.59691664A>G , CM000665.1:g.59691664A>G GRCh37
NC_000003.10:g.59666704A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002959675.1:n.1218-103794A>G