ClinGen Allele Registry
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Canonical Allele Identifier:
CA210694501
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.80939735T>C
GRCh37
chr10:g.82699491T>C
Linked Data - Sequence & Population
gnomAD v2:
10:82699491 T / C
gnomAD v3:
10:80939735 T / C
gnomAD v4:
chr10-80939735-T-C
Joint Max Group AF
0.22098679 (MID)
Genomes Max Group AF
0.18430787 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1484170
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.80939735T>C , CM000672.2:g.80939735T>C
GRCh38
NC_000010.10:g.82699491T>C , CM000672.1:g.82699491T>C
GRCh37
NC_000010.9:g.82689471T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'