ClinGen Allele Registry
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Canonical Allele Identifier:
CA13222978
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.68259614G>A
GRCh37
chr10:g.70019371G>A
Linked Data - Sequence & Population
gnomAD v2:
10:70019371 G / A
gnomAD v3:
10:68259614 G / A
gnomAD v4:
chr10-68259614-G-A
Joint Max Group AF
0.23126984 (SAS)
Genomes Max Group AF
0.23126984 (SAS)
Linked Data - NCBI & NCI
dbSNP:
12571093
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.68259614G>A , CM000672.2:g.68259614G>A
GRCh38
NC_000010.10:g.70019371G>A , CM000672.1:g.70019371G>A
GRCh37
NC_000010.9:g.69689377G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'