ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10820754
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.192795690G>A
GRCh37
chr1:g.192764820G>A
Linked Data - Sequence & Population
gnomAD v2:
1:192764820 G / A
gnomAD v3:
1:192795690 G / A
gnomAD v4:
chr1-192795690-G-A
Joint Max Group AF
0.17287404 (NFE)
Genomes Max Group AF
0.17287404 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1933695
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.192795690G>A , CM000663.2:g.192795690G>A
GRCh38
NC_000001.10:g.192764820G>A , CM000663.1:g.192764820G>A
GRCh37
NC_000001.9:g.191031443G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'