ClinGen Allele Registry
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Canonical Allele Identifier:
CA14625451
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.9098489T>C
GRCh37
chr18:g.9098487T>C
Linked Data - Sequence & Population
gnomAD v2:
18:9098487 T / C
gnomAD v3:
18:9098489 T / C
gnomAD v4:
chr18-9098489-T-C
Joint Max Group AF
0.4750096 (SAS)
Genomes Max Group AF
0.4750096 (SAS)
Linked Data - NCBI & NCI
dbSNP:
11661859
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.9098489T>C , CM000680.2:g.9098489T>C
GRCh38
NC_000018.9:g.9098487T>C , CM000680.1:g.9098487T>C
GRCh37
NC_000018.8:g.9088487T>C
NCBI36
NG_013355.1:g.860T>C
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