ClinGen Allele Registry
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Canonical Allele Identifier:
CA10782431
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.161215085A>G
GRCh37
chr1:g.161184875A>G
Linked Data - Sequence & Population
gnomAD v2:
1:161184875 A / G
gnomAD v3:
1:161215085 A / G
gnomAD v4:
chr1-161215085-A-G
Joint Max Group AF
0.24038573 (SAS)
Genomes Max Group AF
0.24211132 (SAS)
Exomes Max Group AF
0.23828198 (SAS)
Linked Data - NCBI & NCI
dbSNP:
11587213
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.161215085A>G , CM000663.2:g.161215085A>G
GRCh38
NC_000001.10:g.161184875A>G , CM000663.1:g.161184875A>G
GRCh37
NC_000001.9:g.159451499A>G
NCBI36
NG_013352.1:g.20771A>G
NG_029043.1:g.4789A>G
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