ClinGen Allele Registry
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Canonical Allele Identifier:
CA215030466
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.117586338C>T
GRCh37
chr10:g.119345849C>T
Linked Data - Sequence & Population
gnomAD v2:
10:119345849 C / T
gnomAD v3:
10:117586338 C / T
gnomAD v4:
chr10-117586338-C-T
Joint Max Group AF
0.00090604 (EAS)
Genomes Max Group AF
0.00090604 (EAS)
Linked Data - NCBI & NCI
dbSNP:
183316690
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.117586338C>T , CM000672.2:g.117586338C>T
GRCh38
NC_000010.10:g.119345849C>T , CM000672.1:g.119345849C>T
GRCh37
NC_000010.9:g.119335839C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'