ClinGen Allele Registry
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Canonical Allele Identifier:
CA13207712
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.124896430A>C
GRCh37
chr10:g.126584999A>C
Linked Data - Sequence & Population
gnomAD v2:
10:126584999 A / C
gnomAD v3:
10:124896430 A / C
gnomAD v4:
chr10-124896430-A-C
Joint Max Group AF
0.21723945 (AFR)
Genomes Max Group AF
0.21723945 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7900929
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.124896430A>C , CM000672.2:g.124896430A>C
GRCh38
NC_000010.10:g.126584999A>C , CM000672.1:g.126584999A>C
GRCh37
NC_000010.9:g.126574989A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'