ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10936109
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.247415139A>G
GRCh37
chr1:g.247578441A>G
Linked Data - Sequence & Population
gnomAD v2:
1:247578441 A / G
gnomAD v3:
1:247415139 A / G
gnomAD v4:
chr1-247415139-A-G
Joint Max Group AF
0.90360629 (EAS)
Genomes Max Group AF
0.90360629 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2027432
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.247415139A>G , CM000663.2:g.247415139A>G
GRCh38
NC_000001.10:g.247578441A>G , CM000663.1:g.247578441A>G
GRCh37
NC_000001.9:g.245645064A>G
NCBI36
NG_007509.2:g.3967A>G , LRG_197:g.3967A>G
Search 100 bp 5'
Search 100 bp 3'