ClinGen Allele Registry
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Canonical Allele Identifier:
CA10848637
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.157160775A>G
GRCh37
chr1:g.157130566A>G
Linked Data - Sequence & Population
gnomAD v2:
1:157130566 A / G
gnomAD v3:
1:157160775 A / G
gnomAD v4:
chr1-157160775-A-G
Joint Max Group AF
0.80985327 (EAS)
Genomes Max Group AF
0.80985327 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6427356
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.157160775A>G , CM000663.2:g.157160775A>G
GRCh38
NC_000001.10:g.157130566A>G , CM000663.1:g.157130566A>G
GRCh37
NC_000001.9:g.155397190A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'