ClinGen Allele Registry
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Canonical Allele Identifier:
CA13264637
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.42496332T>C
GRCh37
chr10:g.42991780T>C
Linked Data - Sequence & Population
gnomAD v2:
10:42991780 T / C
gnomAD v3:
10:42496332 T / C
gnomAD v4:
chr10-42496332-T-C
Joint Max Group AF
0.8528337 (AFR)
Genomes Max Group AF
0.8528337 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1255372
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.42496332T>C , CM000672.2:g.42496332T>C
GRCh38
NC_000010.10:g.42991780T>C , CM000672.1:g.42991780T>C
GRCh37
NC_000010.9:g.42311786T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'