ClinGen Allele Registry
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Canonical Allele Identifier:
CA853915939
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.60963503T>C
GRCh37
chr8:g.61876062T>C
Linked Data - Sequence & Population
gnomAD v3:
8:60963503 T / C
gnomAD v4:
chr8-60963503-T-C
Linked Data - NCBI & NCI
dbSNP:
1459922931
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.60963503T>C , CM000670.2:g.60963503T>C
GRCh38
NC_000008.10:g.61876062T>C , CM000670.1:g.61876062T>C
GRCh37
NC_000008.9:g.62038616T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'