ClinGen Allele Registry
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Canonical Allele Identifier:
CA14618913
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.8479687C>T
GRCh37
chr18:g.8479685C>T
Linked Data - Sequence & Population
gnomAD v2:
18:8479685 C / T
gnomAD v3:
18:8479687 C / T
gnomAD v4:
chr18-8479687-C-T
Joint Max Group AF
0.12512058 (SAS)
Genomes Max Group AF
0.12512058 (SAS)
Linked Data - NCBI & NCI
dbSNP:
12185468
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.8479687C>T , CM000680.2:g.8479687C>T
GRCh38
NC_000018.9:g.8479685C>T , CM000680.1:g.8479685C>T
GRCh37
NC_000018.8:g.8469685C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'