ClinGen Allele Registry
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Canonical Allele Identifier:
CA669972971
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.92705853C>T
GRCh37
chr10:g.94465610C>T
Linked Data - Sequence & Population
gnomAD v3:
10:92705853 C / T
gnomAD v4:
chr10-92705853-C-T
Linked Data - NCBI & NCI
dbSNP:
1217496516
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.92705853C>T , CM000672.2:g.92705853C>T
GRCh38
NC_000010.10:g.94465610C>T , CM000672.1:g.94465610C>T
GRCh37
NC_000010.9:g.94455590C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'