Canonical Allele Identifier: CA1368255602
Gene: CFAP20DC-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705630A= , CM000665.2:g.59705630A= GRCh38
NC_000003.11:g.59691356A= , CM000665.1:g.59691356A= GRCh37
NC_000003.10:g.59666396A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-104102A=