ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA16048474
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.22633861C>G
GRCh37
chr1:g.22960354C>G
Linked Data - Sequence & Population
gnomAD v2:
1:22960354 C / G
gnomAD v3:
1:22633861 C / G
gnomAD v4:
chr1-22633861-C-G
Joint Max Group AF
0.77756116 (AFR)
Genomes Max Group AF
0.77756116 (AFR)
Linked Data - NCBI & NCI
dbSNP:
665691
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.22633861C>G , CM000663.2:g.22633861C>G
GRCh38
NC_000001.10:g.22960354C>G , CM000663.1:g.22960354C>G
GRCh37
NC_000001.9:g.22832941C>G
NCBI36
NG_007282.1:g.2237C>G , LRG_22:g.2237C>G
Search 100 bp 5'
Search 100 bp 3'