ClinGen Allele Registry
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Canonical Allele Identifier:
CA13203501
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.110426390C>T
GRCh37
chr10:g.112186148C>T
Linked Data - Sequence & Population
gnomAD v2:
10:112186148 C / T
gnomAD v3:
10:110426390 C / T
gnomAD v4:
chr10-110426390-C-T
Joint Max Group AF
0.33009733 (NFE)
Genomes Max Group AF
0.33009733 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11195128
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.110426390C>T , CM000672.2:g.110426390C>T
GRCh38
NC_000010.10:g.112186148C>T , CM000672.1:g.112186148C>T
GRCh37
NC_000010.9:g.112176138C>T
NCBI36
Search 100 bp 5'
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