Canonical Allele Identifier: CA1368255813
Gene: CFAP20DC-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59706003A= , CM000665.2:g.59706003A= GRCh38
NC_000003.11:g.59691729A= , CM000665.1:g.59691729A= GRCh37
NC_000003.10:g.59666769A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002959675.1:n.1218-103729A=