ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10874089
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.22375738T>C
GRCh37
chr1:g.22702231T>C
Linked Data - Sequence & Population
gnomAD v2:
1:22702231 T / C
gnomAD v3:
1:22375738 T / C
gnomAD v4:
chr1-22375738-T-C
Joint Max Group AF
0.31698998 (AFR)
Genomes Max Group AF
0.31698998 (AFR)
Linked Data - NCBI & NCI
dbSNP:
12568930
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.22375738T>C , CM000663.2:g.22375738T>C
GRCh38
NC_000001.10:g.22702231T>C , CM000663.1:g.22702231T>C
GRCh37
NC_000001.9:g.22574818T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'