ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15786558
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr13:g.37491309A>C
GRCh37
chr13:g.38065446A>C
Linked Data - Sequence & Population
gnomAD v2:
13:38065446 A / C
gnomAD v3:
13:37491309 A / C
gnomAD v4:
chr13-37491309-A-C
Joint Max Group AF
0.07971958 (AMR)
Genomes Max Group AF
0.07971958 (AMR)
Linked Data - NCBI & NCI
dbSNP:
9646096
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.37491309A>C , CM000675.2:g.37491309A>C
GRCh38
NC_000013.10:g.38065446A>C , CM000675.1:g.38065446A>C
GRCh37
NC_000013.9:g.36963446A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'