ClinGen Allele Registry
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Canonical Allele Identifier:
CA14704792
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.50916290A>G
GRCh37
chr19:g.51419546A>G
Linked Data - Sequence & Population
gnomAD v2:
19:51419546 A / G
gnomAD v3:
19:50916290 A / G
gnomAD v4:
chr19-50916290-A-G
Joint Max Group AF
0.70005178 (AMR)
Genomes Max Group AF
0.70005178 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1701930
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.50916290A>G , CM000681.2:g.50916290A>G
GRCh38
NC_000019.9:g.51419546A>G , CM000681.1:g.51419546A>G
GRCh37
NC_000019.8:g.56111358A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'