ClinGen Allele Registry
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Canonical Allele Identifier:
CA746624413
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.6786474G>A
GRCh37
chr20:g.6767121G>A
Linked Data - Sequence & Population
gnomAD v3:
20:6786474 G / A
gnomAD v4:
chr20-6786474-G-A
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1412354918
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.6786474G>A , CM000682.2:g.6786474G>A
GRCh38
NC_000020.10:g.6767121G>A , CM000682.1:g.6767121G>A
GRCh37
NC_000020.9:g.6715121G>A
NCBI36
Search 100 bp 5'
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