ClinGen Allele Registry
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Canonical Allele Identifier:
CA14618387
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.1807673G>A
GRCh37
chr18:g.1807674G>A
Linked Data - Sequence & Population
gnomAD v2:
18:1807674 G / A
gnomAD v3:
18:1807673 G / A
gnomAD v4:
chr18-1807673-G-A
Joint Max Group AF
0.55393018 (EAS)
Genomes Max Group AF
0.55393018 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9964595
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.1807673G>A , CM000680.2:g.1807673G>A
GRCh38
NC_000018.9:g.1807674G>A , CM000680.1:g.1807674G>A
GRCh37
NC_000018.8:g.1797674G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'