ClinGen Allele Registry
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Canonical Allele Identifier:
CA14716722
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.51020641A>G
GRCh37
chr19:g.51523897A>G
Linked Data - Sequence & Population
gnomAD v2:
19:51523897 A / G
gnomAD v3:
19:51020641 A / G
gnomAD v4:
chr19-51020641-A-G
Joint Max Group AF
0.90894021 (AFR)
Genomes Max Group AF
0.90894021 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3760738
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.51020641A>G , CM000681.2:g.51020641A>G
GRCh38
NC_000019.9:g.51523897A>G , CM000681.1:g.51523897A>G
GRCh37
NC_000019.8:g.56215709A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'