ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10678782
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.85306326G>A
GRCh37
chr1:g.85772009G>A
Linked Data - Sequence & Population
gnomAD v2:
1:85772009 G / A
gnomAD v3:
1:85306326 G / A
gnomAD v4:
chr1-85306326-G-A
Joint Max Group AF
0.49898796 (EAS)
Genomes Max Group AF
0.49898796 (EAS)
Linked Data - NCBI & NCI
dbSNP:
233100
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.85306326G>A , CM000663.2:g.85306326G>A
GRCh38
NC_000001.10:g.85772009G>A , CM000663.1:g.85772009G>A
GRCh37
NC_000001.9:g.85544597G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'