ClinGen Allele Registry
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Canonical Allele Identifier:
CA884509712
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.100718234A>C
GRCh37
chr1:g.101183790A>C
Linked Data - Sequence & Population
gnomAD v3:
1:100718234 A / C
gnomAD v4:
chr1-100718234-A-C
Linked Data - NCBI & NCI
dbSNP:
1241343567
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.100718234A>C , CM000663.2:g.100718234A>C
GRCh38
NC_000001.10:g.101183790A>C , CM000663.1:g.101183790A>C
GRCh37
NC_000001.9:g.100956378A>C
NCBI36
NG_023034.2:g.3494A>C
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