ClinGen Allele Registry
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Canonical Allele Identifier:
CA212071601
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.92705751T>C
GRCh37
chr10:g.94465508T>C
Linked Data - Sequence & Population
gnomAD v3:
10:92705751 T / C
gnomAD v4:
chr10-92705751-T-C
Linked Data - NCBI & NCI
dbSNP:
955703766
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.92705751T>C , CM000672.2:g.92705751T>C
GRCh38
NC_000010.10:g.94465508T>C , CM000672.1:g.94465508T>C
GRCh37
NC_000010.9:g.94455488T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'