ClinGen Allele Registry
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Canonical Allele Identifier:
CA634187991
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.3667726A>C
GRCh37
chr20:g.3648373A>C
Linked Data - Sequence & Population
gnomAD v2:
20:3648373 A / C
gnomAD v3:
20:3667726 A / C
gnomAD v4:
chr20-3667726-A-C
Linked Data - NCBI & NCI
dbSNP:
1294626107
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.3667726A>C , CM000682.2:g.3667726A>C
GRCh38
NC_000020.10:g.3648373A>C , CM000682.1:g.3648373A>C
GRCh37
NC_000020.9:g.3596373A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'