ClinGen Allele Registry
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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
MyVariant Identifiers:
chr3:g.59691603T>G (hg19)
chr3:g.59705877T>G (hg38)
JSON-LD
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
Search 100 bp 5'
Search 100 bp 3'