ClinGen Allele Registry
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Canonical Allele Identifier:
CA14755889
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.37439987A>C
GRCh37
chr20:g.36068389A>C
Linked Data - Sequence & Population
gnomAD v2:
20:36068389 A / C
gnomAD v3:
20:37439987 A / C
gnomAD v4:
chr20-37439987-A-C
Joint Max Group AF
0.25818036 (EAS)
Genomes Max Group AF
0.25818036 (EAS)
Linked Data - NCBI & NCI
dbSNP:
17194885
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.37439987A>C , CM000682.2:g.37439987A>C
GRCh38
NC_000020.10:g.36068389A>C , CM000682.1:g.36068389A>C
GRCh37
NC_000020.9:g.35501803A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'