Canonical Allele Identifier: CA908843493
Gene: CFAP20DC-DT HGNC NCBI

Linked Data

dbSNP Id: rs1449656499
gnomAD v3: 3-59705877-T-G
gnomAD v4: 3-59705877-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.59705877T>G , CM000665.2:g.59705877T>G GRCh38
NC_000003.11:g.59691603T>G , CM000665.1:g.59691603T>G GRCh37
NC_000003.10:g.59666643T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959675.1:n.1218-103855T>G