ClinGen Allele Registry
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Canonical Allele Identifier:
CA31395086
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.159730249A>G
GRCh37
chr1:g.159700039A>G
Linked Data - Sequence & Population
gnomAD v2:
1:159700039 A / G
gnomAD v3:
1:159730249 A / G
gnomAD v4:
chr1-159730249-A-G
Joint Max Group AF
0.14286818 (EAS)
Genomes Max Group AF
0.14286818 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11265260
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.159730249A>G , CM000663.2:g.159730249A>G
GRCh38
NC_000001.10:g.159700039A>G , CM000663.1:g.159700039A>G
GRCh37
NC_000001.9:g.157966663A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'