Canonical Allele Identifier: CA908843448
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1448833607
gnomAD v3: 3-59705800-G-C
gnomAD v4: 3-59705800-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705800G>C , CM000665.2:g.59705800G>C GRCh38
NC_000003.11:g.59691526G>C , CM000665.1:g.59691526G>C GRCh37
NC_000003.10:g.59666566G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103932G>C