ClinGen Allele Registry
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Canonical Allele Identifier:
CA10842110
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.80327433A>G
GRCh37
chr1:g.80793118A>G
Linked Data - Sequence & Population
gnomAD v2:
1:80793118 A / G
gnomAD v3:
1:80327433 A / G
gnomAD v4:
chr1-80327433-A-G
Joint Max Group AF
0.34867817 (SAS)
Genomes Max Group AF
0.34867817 (SAS)
Linked Data - NCBI & NCI
dbSNP:
12065553
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.80327433A>G , CM000663.2:g.80327433A>G
GRCh38
NC_000001.10:g.80793118A>G , CM000663.1:g.80793118A>G
GRCh37
NC_000001.9:g.80565706A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'