ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10943871
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.190097256T>C
GRCh37
chr1:g.190066386T>C
Linked Data - Sequence & Population
gnomAD v2:
1:190066386 T / C
gnomAD v3:
1:190097256 T / C
gnomAD v4:
chr1-190097256-T-C
Joint Max Group AF
0.3516126 (NFE)
Genomes Max Group AF
0.3516126 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1935881
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.190097256T>C , CM000663.2:g.190097256T>C
GRCh38
NC_000001.10:g.190066386T>C , CM000663.1:g.190066386T>C
GRCh37
NC_000001.9:g.188333009T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'