ClinGen Allele Registry
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Canonical Allele Identifier:
CA15132258
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.155159197A>G
GRCh37
chr1:g.155131673A>G
Linked Data - Sequence & Population
gnomAD v2:
1:155131673 A / G
gnomAD v3:
1:155159197 A / G
gnomAD v4:
chr1-155159197-A-G
Joint Max Group AF
0.79729097 (EAS)
Genomes Max Group AF
0.79729097 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4276913
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.155159197A>G , CM000663.2:g.155159197A>G
GRCh38
NC_000001.10:g.155131673A>G , CM000663.1:g.155131673A>G
GRCh37
NC_000001.9:g.153398297A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'