ClinGen Allele Registry
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Canonical Allele Identifier:
CA303995920
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.1106937A>G
GRCh37
chr19:g.1106936A>G
Linked Data - Sequence & Population
gnomAD v2:
19:1106936 A / G
gnomAD v3:
19:1106937 A / G
gnomAD v4:
chr19-1106937-A-G
Joint Max Group AF
0.00010528 (NFE)
Genomes Max Group AF
0.00011228 (NFE)
Exomes Max Group AF
0.00008924 (NFE)
Linked Data - NCBI & NCI
dbSNP:
776428688
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1106937A>G , CM000681.2:g.1106937A>G
GRCh38
NC_000019.9:g.1106936A>G , CM000681.1:g.1106936A>G
GRCh37
NC_000019.8:g.1057936A>G
NCBI36
NG_050621.1:g.8012A>G
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