Canonical Allele Identifier: CA908843531
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1309129191

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705974G>C , CM000665.2:g.59705974G>C GRCh38
NC_000003.11:g.59691700G>C , CM000665.1:g.59691700G>C GRCh37
NC_000003.10:g.59666740G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103758G>C