Canonical Allele Identifier: CA908843397
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs978839370
gnomAD v3: 3-59705747-A-C
gnomAD v4: 3-59705747-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705747A>C , CM000665.2:g.59705747A>C GRCh38
NC_000003.11:g.59691473A>C , CM000665.1:g.59691473A>C GRCh37
NC_000003.10:g.59666513A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103985A>C