ClinGen Allele Registry
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Canonical Allele Identifier:
CA16056782
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.70529879G>A
GRCh37
chr1:g.70995562G>A
Linked Data - Sequence & Population
gnomAD v2:
1:70995562 G / A
gnomAD v3:
1:70529879 G / A
gnomAD v4:
chr1-70529879-G-A
Joint Max Group AF
0.38335841 (NFE)
Genomes Max Group AF
0.38335841 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2651244
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.70529879G>A , CM000663.2:g.70529879G>A
GRCh38
NC_000001.10:g.70995562G>A , CM000663.1:g.70995562G>A
GRCh37
NC_000001.9:g.70768150G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'