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Canonical Allele Identifier:
CA14512541
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.26757460C>G
GRCh37
chr18:g.24337424C>G
Linked Data - Sequence & Population
gnomAD v2:
18:24337424 C / G
gnomAD v3:
18:26757460 C / G
gnomAD v4:
chr18-26757460-C-G
Joint Max Group AF
0.85792435 (AFR)
Genomes Max Group AF
0.85792435 (AFR)
Linked Data - NCBI & NCI
dbSNP:
527616
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.26757460C>G , CM000680.2:g.26757460C>G
GRCh38
NC_000018.9:g.24337424C>G , CM000680.1:g.24337424C>G
GRCh37
NC_000018.8:g.22591422C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'