ClinGen Allele Registry
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Canonical Allele Identifier:
CA12589602
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.71008019C>T
GRCh37
chr7:g.70473005C>T
Linked Data - Sequence & Population
gnomAD v2:
7:70473005 C / T
gnomAD v3:
7:71008019 C / T
gnomAD v4:
chr7-71008019-C-T
Joint Max Group AF
0.44919674 (EAS)
Genomes Max Group AF
0.44919674 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1525293
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.71008019C>T , CM000669.2:g.71008019C>T
GRCh38
NC_000007.13:g.70473005C>T , CM000669.1:g.70473005C>T
GRCh37
NC_000007.12:g.70110941C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'