ClinGen Allele Registry
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Canonical Allele Identifier:
CA211723596
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.94935323T>C
GRCh37
chr10:g.96695080T>C
Linked Data - Sequence & Population
gnomAD v2:
10:96695080 T / C
gnomAD v3:
10:94935323 T / C
gnomAD v4:
chr10-94935323-T-C
Joint Max Group AF
0.20989809 (AFR)
Genomes Max Group AF
0.20989809 (AFR)
Linked Data - NCBI & NCI
dbSNP:
61886769
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.94935323T>C , CM000672.2:g.94935323T>C
GRCh38
NC_000010.10:g.96695080T>C , CM000672.1:g.96695080T>C
GRCh37
NC_000010.9:g.96685070T>C
NCBI36
NG_008385.1:g.1666T>C
NG_008385.2:g.2166T>C
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