ClinGen Allele Registry
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Canonical Allele Identifier:
CA14722312
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.43782361A>G
GRCh37
chr19:g.44286513A>G
Linked Data - Sequence & Population
gnomAD v2:
19:44286513 A / G
gnomAD v3:
19:43782361 A / G
gnomAD v4:
chr19-43782361-A-G
Joint Max Group AF
0.82071241 (EAS)
Genomes Max Group AF
0.82071241 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3760982
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.43782361A>G , CM000681.2:g.43782361A>G
GRCh38
NC_000019.9:g.44286513A>G , CM000681.1:g.44286513A>G
GRCh37
NC_000019.8:g.48978353A>G
NCBI36
NG_052672.1:g.4779T>C
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