ClinGen Allele Registry
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Canonical Allele Identifier:
CA13179478
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.4613373A>G
GRCh37
chr10:g.4655565A>G
Linked Data - Sequence & Population
gnomAD v2:
10:4655565 A / G
gnomAD v3:
10:4613373 A / G
gnomAD v4:
chr10-4613373-A-G
Joint Max Group AF
0.97266313 (EAS)
Genomes Max Group AF
0.97266313 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10458787
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.4613373A>G , CM000672.2:g.4613373A>G
GRCh38
NC_000010.10:g.4655565A>G , CM000672.1:g.4655565A>G
GRCh37
NC_000010.9:g.4645565A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'