ClinGen Allele Registry
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Canonical Allele Identifier:
CA10820756
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.192808434A>G
GRCh37
chr1:g.192777564A>G
Linked Data - Sequence & Population
gnomAD v2:
1:192777564 A / G
gnomAD v3:
1:192808434 A / G
gnomAD v4:
chr1-192808434-A-G
Joint Max Group AF
0.48089372 (EAS)
Genomes Max Group AF
0.48089372 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2746071
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.192808434A>G , CM000663.2:g.192808434A>G
GRCh38
NC_000001.10:g.192777564A>G , CM000663.1:g.192777564A>G
GRCh37
NC_000001.9:g.191044187A>G
NCBI36
NG_012800.1:g.4396A>G
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