ClinGen Allele Registry
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Canonical Allele Identifier:
CA27681483
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.100718244A>C
GRCh37
chr1:g.101183800A>C
Linked Data - Sequence & Population
gnomAD v2:
1:101183800 A / C
gnomAD v3:
1:100718244 A / C
gnomAD v4:
chr1-100718244-A-C
Joint Max Group AF
0.0001667 (AFR)
Genomes Max Group AF
0.0001667 (AFR)
Linked Data - NCBI & NCI
dbSNP:
889032730
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.100718244A>C , CM000663.2:g.100718244A>C
GRCh38
NC_000001.10:g.101183800A>C , CM000663.1:g.101183800A>C
GRCh37
NC_000001.9:g.100956388A>C
NCBI36
NG_023034.2:g.3504A>C
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