ClinGen Allele Registry
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Canonical Allele Identifier:
CA14683702
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.12890733A>G
GRCh37
chr19:g.13001547A>G
Linked Data - Sequence & Population
gnomAD v2:
19:13001547 A / G
gnomAD v3:
19:12890733 A / G
gnomAD v4:
chr19-12890733-A-G
Joint Max Group AF
0.36750248 (AMR)
Genomes Max Group AF
0.36750248 (AMR)
Linked Data - NCBI & NCI
dbSNP:
11085824
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.12890733A>G , CM000681.2:g.12890733A>G
GRCh38
NC_000019.9:g.13001547A>G , CM000681.1:g.13001547A>G
GRCh37
NC_000019.8:g.12862547A>G
NCBI36
NG_009292.1:g.4574A>G
NG_013087.1:g.1471T>C
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