ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
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
MyVariant Identifiers:
chr3:g.59691725G>A (hg19)
chr3:g.59705999G>A (hg38)
JSON-LD
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
Search 100 bp 5'
Search 100 bp 3'