ClinGen Allele Registry
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Canonical Allele Identifier:
CA10655966
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.2961801G>A
GRCh37
chr1:g.2878366G>A
Linked Data - Sequence & Population
gnomAD v2:
1:2878366 G / A
gnomAD v3:
1:2961801 G / A
gnomAD v4:
chr1-2961801-G-A
Joint Max Group AF
0.56475874 (NFE)
Genomes Max Group AF
0.56482287 (NFE)
Exomes Max Group AF
0.2787758 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11583804
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.2961801G>A , CM000663.2:g.2961801G>A
GRCh38
NC_000001.10:g.2878366G>A , CM000663.1:g.2878366G>A
GRCh37
NC_000001.9:g.2868226G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'