ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA16476157
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.86590602C>T
GRCh37
chr13:g.87242857C>T
Linked Data - Sequence & Population
gnomAD v2:
13:87242857 C / T
gnomAD v3:
13:86590602 C / T
gnomAD v4:
chr13-86590602-C-T
Joint Max Group AF
0.4446346 (AFR)
Genomes Max Group AF
0.4446346 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4773460
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.86590602C>T , CM000675.2:g.86590602C>T
GRCh38
NC_000013.10:g.87242857C>T , CM000675.1:g.87242857C>T
GRCh37
NC_000013.9:g.86040858C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'