ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15217270
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.5767748T>C
GRCh37
chr2:g.5907880T>C
Linked Data - Sequence & Population
gnomAD v2:
2:5907880 T / C
gnomAD v3:
2:5767748 T / C
gnomAD v4:
chr2-5767748-T-C
Joint Max Group AF
0.13554672 (SAS)
Genomes Max Group AF
0.13554672 (SAS)
Linked Data - NCBI & NCI
dbSNP:
16864170
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.5767748T>C , CM000664.2:g.5767748T>C
GRCh38
NC_000002.11:g.5907880T>C , CM000664.1:g.5907880T>C
GRCh37
NC_000002.10:g.5825331T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'