ClinGen Allele Registry
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Canonical Allele Identifier:
CA14738929
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.7668969G>A
GRCh37
chr19:g.7733855G>A
Linked Data - Sequence & Population
gnomAD v2:
19:7733855 G / A
gnomAD v3:
19:7668969 G / A
gnomAD v4:
chr19-7668969-G-A
Joint Max Group AF
0.17497716 (EAS)
Genomes Max Group AF
0.17822292 (EAS)
Exomes Max Group AF
0.16831272 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3219175
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.7668969G>A , CM000681.2:g.7668969G>A
GRCh38
NC_000019.9:g.7733855G>A , CM000681.1:g.7733855G>A
GRCh37
NC_000019.8:g.7639855G>A
NCBI36
NG_023447.1:g.4884G>A
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