ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13560260
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.56474785G>T
GRCh37
chr11:g.56242261G>T
Linked Data - Sequence & Population
gnomAD v2:
11:56242261 G / T
gnomAD v3:
11:56474785 G / T
gnomAD v4:
chr11-56474785-G-T
Joint Max Group AF
0.13402675 (EAS)
Genomes Max Group AF
0.13402675 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7939886
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.56474785G>T , CM000673.2:g.56474785G>T
GRCh38
NC_000011.9:g.56242261G>T , CM000673.1:g.56242261G>T
GRCh37
NC_000011.8:g.55998837G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'