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Canonical Allele Identifier:
CA11498074
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.36814539T>C
GRCh37
chr3:g.36856030T>C
Linked Data - Sequence & Population
gnomAD v2:
3:36856030 T / C
gnomAD v3:
3:36814539 T / C
gnomAD v4:
chr3-36814539-T-C
Joint Max Group AF
0.58726494 (EAS)
Genomes Max Group AF
0.58726494 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9834970
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.36814539T>C , CM000665.2:g.36814539T>C
GRCh38
NC_000003.11:g.36856030T>C , CM000665.1:g.36856030T>C
GRCh37
NC_000003.10:g.36831034T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'