ClinGen Allele Registry
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Canonical Allele Identifier:
CA14569924
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr18:g.22643732C>A
GRCh37
chr18:g.20223695C>A
Linked Data - Sequence & Population
gnomAD v2:
18:20223695 C / A
gnomAD v3:
18:22643732 C / A
gnomAD v4:
chr18-22643732-C-A
Joint Max Group AF
0.50707203 (NFE)
Genomes Max Group AF
0.50707203 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11661542
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.22643732C>A , CM000680.2:g.22643732C>A
GRCh38
NC_000018.9:g.20223695C>A , CM000680.1:g.20223695C>A
GRCh37
NC_000018.8:g.18477693C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'