ClinGen Allele Registry
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Canonical Allele Identifier:
CA297701627
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr18:g.31607316A>C
GRCh37
chr18:g.29187279A>C
Linked Data - Sequence & Population
gnomAD v2:
18:29187279 A / C
gnomAD v3:
18:31607316 A / C
gnomAD v4:
chr18-31607316-A-C
Joint Max Group AF
0.69653341 (AFR)
Genomes Max Group AF
0.69653341 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1667255
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.31607316A>C , CM000680.2:g.31607316A>C
GRCh38
NC_000018.9:g.29187279A>C , CM000680.1:g.29187279A>C
GRCh37
NC_000018.8:g.27441277A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'