ClinGen Allele Registry
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Canonical Allele Identifier:
CA13265476
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.45373441G>A
GRCh37
chr10:g.45868889G>A
Linked Data - Sequence & Population
gnomAD v2:
10:45868889 G / A
gnomAD v3:
10:45373441 G / A
gnomAD v4:
chr10-45373441-G-A
Joint Max Group AF
0.17913139 (SAS)
Genomes Max Group AF
0.17913139 (SAS)
Linked Data - NCBI & NCI
dbSNP:
7913948
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.45373441G>A , CM000672.2:g.45373441G>A
GRCh38
NC_000010.10:g.45868889G>A , CM000672.1:g.45868889G>A
GRCh37
NC_000010.9:g.45188895G>A
NCBI36
NG_011437.1:g.4261G>A
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