ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12291793
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.29685409A>G
GRCh37
chr6:g.29653186A>G
Linked Data - Sequence & Population
gnomAD v2:
6:29653186 A / G
gnomAD v3:
6:29685409 A / G
gnomAD v4:
chr6-29685409-A-G
Joint Max Group AF
0.41475403 (AFR)
Genomes Max Group AF
0.41475403 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2747442
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.29685409A>G , CM000668.2:g.29685409A>G
GRCh38
NC_000006.11:g.29653186A>G , CM000668.1:g.29653186A>G
GRCh37
NC_000006.10:g.29761165A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'