ClinGen Allele Registry
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Canonical Allele Identifier:
CA27681442
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.100718209A>G
GRCh37
chr1:g.101183765A>G
Linked Data - Sequence & Population
gnomAD v2:
1:101183765 A / G
gnomAD v3:
1:100718209 A / G
gnomAD v4:
chr1-100718209-A-G
Joint Max Group AF
0.00214598 (AMR)
Genomes Max Group AF
0.00214598 (AMR)
Linked Data - NCBI & NCI
dbSNP:
549035796
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.100718209A>G , CM000663.2:g.100718209A>G
GRCh38
NC_000001.10:g.101183765A>G , CM000663.1:g.101183765A>G
GRCh37
NC_000001.9:g.100956353A>G
NCBI36
NG_023034.2:g.3469A>G
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