ClinGen Allele Registry
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Canonical Allele Identifier:
CA10658853
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.8257898A>C
GRCh37
chr1:g.8317958A>C
Linked Data - Sequence & Population
gnomAD v2:
1:8317958 A / C
gnomAD v3:
1:8257898 A / C
gnomAD v4:
chr1-8257898-A-C
Joint Max Group AF
0.79830355 (NFE)
Genomes Max Group AF
0.79830355 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7520292
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.8257898A>C , CM000663.2:g.8257898A>C
GRCh38
NC_000001.10:g.8317958A>C , CM000663.1:g.8317958A>C
GRCh37
NC_000001.9:g.8240545A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'