ClinGen Allele Registry
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Canonical Allele Identifier:
CA745270584
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.50758705A>C
GRCh37
chr20:g.49375242A>C
Linked Data - Sequence & Population
gnomAD v3:
20:50758705 A / C
gnomAD v4:
chr20-50758705-A-C
Linked Data - NCBI & NCI
dbSNP:
6122972
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.50758705A>C , CM000682.2:g.50758705A>C
GRCh38
NC_000020.10:g.49375242A>C , CM000682.1:g.49375242A>C
GRCh37
NC_000020.9:g.48808649A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'