ClinGen Allele Registry
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Canonical Allele Identifier:
CA304895972
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.7668790A>C
GRCh37
chr19:g.7733676A>C
Linked Data - Sequence & Population
gnomAD v2:
19:7733676 A / C
gnomAD v3:
19:7668790 A / C
gnomAD v4:
chr19-7668790-A-C
Joint Max Group AF
0.09833102 (EAS)
Genomes Max Group AF
0.09833102 (EAS)
Linked Data - NCBI & NCI
dbSNP:
34124816
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.7668790A>C , CM000681.2:g.7668790A>C
GRCh38
NC_000019.9:g.7733676A>C , CM000681.1:g.7733676A>C
GRCh37
NC_000019.8:g.7639676A>C
NCBI36
NG_023447.1:g.4705A>C
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