ClinGen Allele Registry
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Canonical Allele Identifier:
CA10942503
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.160887174A>G
GRCh37
chr1:g.160856964A>G
Linked Data - Sequence & Population
gnomAD v2:
1:160856964 A / G
gnomAD v3:
1:160887174 A / G
gnomAD v4:
chr1-160887174-A-G
Joint Max Group AF
0.7001179 (EAS)
Genomes Max Group AF
0.7001179 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4656958
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.160887174A>G , CM000663.2:g.160887174A>G
GRCh38
NC_000001.10:g.160856964A>G , CM000663.1:g.160856964A>G
GRCh37
NC_000001.9:g.159123588A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'