ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10692865
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.177886382C>A
GRCh37
chr1:g.177855517C>A
Linked Data - Sequence & Population
gnomAD v2:
1:177855517 C / A
gnomAD v3:
1:177886382 C / A
gnomAD v4:
chr1-177886382-C-A
Joint Max Group AF
0.19288906 (NFE)
Genomes Max Group AF
0.19288906 (NFE)
Linked Data - NCBI & NCI
dbSNP:
516636
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.177886382C>A , CM000663.2:g.177886382C>A
GRCh38
NC_000001.10:g.177855517C>A , CM000663.1:g.177855517C>A
GRCh37
NC_000001.9:g.176122140C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'