Canonical Allele Identifier: CA1368255632
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1700183039

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705670C>A , CM000665.2:g.59705670C>A GRCh38
NC_000003.11:g.59691396C>A , CM000665.1:g.59691396C>A GRCh37
NC_000003.10:g.59666436C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-104062C>A