ClinGen Allele Registry
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Canonical Allele Identifier:
CA27681408
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.100718159C>A
GRCh37
chr1:g.101183715C>A
Linked Data - Sequence & Population
gnomAD v3:
1:100718159 C / A
gnomAD v4:
chr1-100718159-C-A
Linked Data - NCBI & NCI
dbSNP:
539081700
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.100718159C>A , CM000663.2:g.100718159C>A
GRCh38
NC_000001.10:g.101183715C>A , CM000663.1:g.101183715C>A
GRCh37
NC_000001.9:g.100956303C>A
NCBI36
NG_023034.2:g.3419C>A
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