ClinGen Allele Registry
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Canonical Allele Identifier:
CA10790243
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.218532419A>C
GRCh37
chr1:g.218705761A>C
Linked Data - Sequence & Population
gnomAD v2:
1:218705761 A / C
gnomAD v3:
1:218532419 A / C
gnomAD v4:
chr1-218532419-A-C
Joint Max Group AF
0.30669202 (EAS)
Genomes Max Group AF
0.30669202 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11118120
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.218532419A>C , CM000663.2:g.218532419A>C
GRCh38
NC_000001.10:g.218705761A>C , CM000663.1:g.218705761A>C
GRCh37
NC_000001.9:g.216772384A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'