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Canonical Allele Identifier:
CA11995331
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.10169711T>C
GRCh37
chr5:g.10169823T>C
Linked Data - Sequence & Population
gnomAD v2:
5:10169823 T / C
gnomAD v3:
5:10169711 T / C
gnomAD v4:
chr5-10169711-T-C
Joint Max Group AF
0.43419379 (AMR)
Genomes Max Group AF
0.43419379 (AMR)
Linked Data - NCBI & NCI
dbSNP:
13361160
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.10169711T>C , CM000667.2:g.10169711T>C
GRCh38
NC_000005.9:g.10169823T>C , CM000667.1:g.10169823T>C
GRCh37
NC_000005.8:g.10222823T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'