Canonical Allele Identifier: CA1048502776
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1700186761
gnomAD v3: 3-59706028-C-T
gnomAD v4: 3-59706028-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59706028C>T , CM000665.2:g.59706028C>T GRCh38
NC_000003.11:g.59691754C>T , CM000665.1:g.59691754C>T GRCh37
NC_000003.10:g.59666794C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103704C>T