ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10979201
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.161302651A>G
GRCh37
chr1:g.161272441A>G
Linked Data - Sequence & Population
gnomAD v2:
1:161272441 A / G
gnomAD v3:
1:161302651 A / G
gnomAD v4:
chr1-161302651-A-G
Joint Max Group AF
0.70765831 (EAS)
Genomes Max Group AF
0.70765831 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4657015
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.161302651A>G , CM000663.2:g.161302651A>G
GRCh38
NC_000001.10:g.161272441A>G , CM000663.1:g.161272441A>G
GRCh37
NC_000001.9:g.159539065A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'