Canonical Allele Identifier: CA1368255818
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1700186620
gnomAD v3: 3-59706017-A-G
gnomAD v4: 3-59706017-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59706017A>G , CM000665.2:g.59706017A>G GRCh38
NC_000003.11:g.59691743A>G , CM000665.1:g.59691743A>G GRCh37
NC_000003.10:g.59666783A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103715A>G