ClinGen Allele Registry
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Canonical Allele Identifier:
CA21833167
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.45329029del
GRCh37
chr1:g.45794701del
Linked Data - Sequence & Population
gnomAD v2:
1:45794700 TC / T
gnomAD v3:
1:45329028 TC / T
gnomAD v4:
chr1-45329028-TC-T
Joint Max Group AF
0.00007534 (NFE)
Genomes Max Group AF
0.0000681 (NFE)
Exomes Max Group AF
0.00006217 (NFE)
Linked Data - NCBI & NCI
dbSNP:
768252333
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.45329031del , CM000663.2:g.45329031del
GRCh38
NC_000001.10:g.45794703del , CM000663.1:g.45794703del
GRCh37
NC_000001.9:g.45567290del
NCBI36
NG_008189.1:g.16442del , LRG_220:g.16442del
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