Canonical Allele Identifier: CA11444608
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs17061085
gnomAD v2: 3-59691725-G-A
gnomAD v3: 3-59705999-G-A
gnomAD v4: 3-59705999-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705999G>A , CM000665.2:g.59705999G>A GRCh38
NC_000003.11:g.59691725G>A , CM000665.1:g.59691725G>A GRCh37
NC_000003.10:g.59666765G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002959675.1:n.1218-103733G>A