ClinGen Allele Registry
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Canonical Allele Identifier:
CA14549089
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.48868651A>G
GRCh37
chr18:g.46395022A>G
Linked Data - Sequence & Population
gnomAD v2:
18:46395022 A / G
gnomAD v3:
18:48868651 A / G
gnomAD v4:
chr18-48868651-A-G
Joint Max Group AF
0.52976894 (AFR)
Genomes Max Group AF
0.52976894 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7240004
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.48868651A>G , CM000680.2:g.48868651A>G
GRCh38
NC_000018.9:g.46395022A>G , CM000680.1:g.46395022A>G
GRCh37
NC_000018.8:g.44649020A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'