ClinGen Allele Registry
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Canonical Allele Identifier:
CA15673979
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.94937495T>C
GRCh37
chr10:g.96697252T>C
Linked Data - Sequence & Population
gnomAD v2:
10:96697252 T / C
gnomAD v3:
10:94937495 T / C
gnomAD v4:
chr10-94937495-T-C
Joint Max Group AF
0.46211789 (SAS)
Genomes Max Group AF
0.46211789 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4918758
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.94937495T>C , CM000672.2:g.94937495T>C
GRCh38
NC_000010.10:g.96697252T>C , CM000672.1:g.96697252T>C
GRCh37
NC_000010.9:g.96687242T>C
NCBI36
NG_008385.1:g.3838T>C
NG_008385.2:g.4338T>C
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