ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15421982
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.29966386A>C
GRCh37
chr6:g.29934163A>C
Linked Data - Sequence & Population
gnomAD v2:
6:29934163 A / C
gnomAD v3:
6:29966386 A / C
gnomAD v4:
chr6-29966386-A-C
Joint Max Group AF
0.29974644 (EAS)
Genomes Max Group AF
0.29974644 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6935053
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.29966386A>C , CM000668.2:g.29966386A>C
GRCh38
NC_000006.11:g.29934163A>C , CM000668.1:g.29934163A>C
GRCh37
NC_000006.10:g.30042142A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'