ClinGen Allele Registry
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Canonical Allele Identifier:
CA10736156
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.109276674C>A
GRCh37
chr1:g.109819296C>A
Linked Data - Sequence & Population
gnomAD v2:
1:109819296 C / A
gnomAD v3:
1:109276674 C / A
gnomAD v4:
chr1-109276674-C-A
Joint Max Group AF
0.91005179 (EAS)
Genomes Max Group AF
0.91005179 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3902354
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.109276674C>A , CM000663.2:g.109276674C>A
GRCh38
NC_000001.10:g.109819296C>A , CM000663.1:g.109819296C>A
GRCh37
NC_000001.9:g.109620819C>A
NCBI36
NG_052669.1:g.31970C>A
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