ClinGen Allele Registry
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Canonical Allele Identifier:
CA10984463
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.59278242G>A
GRCh37
chr1:g.59743914G>A
Linked Data - Sequence & Population
gnomAD v2:
1:59743914 G / A
gnomAD v3:
1:59278242 G / A
gnomAD v4:
chr1-59278242-G-A
Joint Max Group AF
0.97516648 (EAS)
Genomes Max Group AF
0.97516648 (EAS)
Linked Data - NCBI & NCI
dbSNP:
333662
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.59278242G>A , CM000663.2:g.59278242G>A
GRCh38
NC_000001.10:g.59743914G>A , CM000663.1:g.59743914G>A
GRCh37
NC_000001.9:g.59516502G>A
NCBI36
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