ClinGen Allele Registry
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Canonical Allele Identifier:
CA12265922
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.31382927C>T
GRCh37
chr6:g.31350704C>T
Linked Data - Sequence & Population
gnomAD v2:
6:31350704 C / T
gnomAD v3:
6:31382927 C / T
gnomAD v4:
chr6-31382927-C-T
Joint Max Group AF
0.90280371 (EAS)
Genomes Max Group AF
0.90280371 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1521
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31382927C>T , CM000668.2:g.31382927C>T
GRCh38
NC_000006.11:g.31350704C>T , CM000668.1:g.31350704C>T
GRCh37
NC_000006.10:g.31458683C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'