Canonical Allele Identifier: CA1048502781
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1700186806
gnomAD v3: 3-59706038-G-A
gnomAD v4: 3-59706038-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59706038G>A , CM000665.2:g.59706038G>A GRCh38
NC_000003.11:g.59691764G>A , CM000665.1:g.59691764G>A GRCh37
NC_000003.10:g.59666804G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002959675.1:n.1218-103694G>A