ClinGen Allele Registry
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Canonical Allele Identifier:
CA773378863
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.56695877T>A
GRCh37
chr17:g.54773238T>A
Linked Data - Sequence & Population
gnomAD v3:
17:56695877 T / A
gnomAD v4:
chr17-56695877-T-A
Joint Max Group AF
0.00000801 (AFR)
Genomes Max Group AF
0.00000801 (AFR)
Linked Data - NCBI & NCI
dbSNP:
227731
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.56695877T>A , CM000679.2:g.56695877T>A
GRCh38
NC_000017.10:g.54773238T>A , CM000679.1:g.54773238T>A
GRCh37
NC_000017.9:g.52128237T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'