ClinGen Allele Registry
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Canonical Allele Identifier:
CA12403219
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.82696390C>T
GRCh37
chr6:g.83406107C>T
Linked Data - Sequence & Population
gnomAD v2:
6:83406107 C / T
gnomAD v3:
6:82696390 C / T
gnomAD v4:
chr6-82696390-C-T
Joint Max Group AF
0.74395818 (EAS)
Genomes Max Group AF
0.74395818 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1547251
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.82696390C>T , CM000668.2:g.82696390C>T
GRCh38
NC_000006.11:g.83406107C>T , CM000668.1:g.83406107C>T
GRCh37
NC_000006.10:g.83462826C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'