ClinGen Allele Registry
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Canonical Allele Identifier:
CA215030483
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.117586473C>A
GRCh37
chr10:g.119345984C>A
Linked Data - Sequence & Population
gnomAD v3:
10:117586473 C / A
gnomAD v4:
chr10-117586473-C-A
Linked Data - NCBI & NCI
dbSNP:
747669359
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.117586473C>A , CM000672.2:g.117586473C>A
GRCh38
NC_000010.10:g.119345984C>A , CM000672.1:g.119345984C>A
GRCh37
NC_000010.9:g.119335974C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'