ClinGen Allele Registry
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Canonical Allele Identifier:
CA304896006
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.7668907C>T
GRCh37
chr19:g.7733793C>T
Linked Data - Sequence & Population
gnomAD v2:
19:7733793 C / T
gnomAD v3:
19:7668907 C / T
gnomAD v4:
chr19-7668907-C-T
Joint Max Group AF
0.00160344 (AFR)
Genomes Max Group AF
0.00160996 (AFR)
Exomes Max Group AF
0.00142681 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1862513
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.7668907C>T , CM000681.2:g.7668907C>T
GRCh38
NC_000019.9:g.7733793C>T , CM000681.1:g.7733793C>T
GRCh37
NC_000019.8:g.7639793C>T
NCBI36
NG_023447.1:g.4822C>T
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