ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13398338
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.116827022C>A
GRCh37
chr11:g.116697738C>A
Linked Data - Sequence & Population
gnomAD v2:
11:116697738 C / A
gnomAD v3:
11:116827022 C / A
gnomAD v4:
chr11-116827022-C-A
Joint Max Group AF
0.6242183 (NFE)
Genomes Max Group AF
0.6242183 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2542051
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.116827022C>A , CM000673.2:g.116827022C>A
GRCh38
NC_000011.9:g.116697738C>A , CM000673.1:g.116697738C>A
GRCh37
NC_000011.8:g.116202948C>A
NCBI36
NG_008949.1:g.2115C>A
NG_012044.1:g.1274G>T
Search 100 bp 5'
Search 100 bp 3'