ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12783449
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.6883416A>G
GRCh37
chr8:g.6740938A>G
Linked Data - Sequence & Population
gnomAD v2:
8:6740938 A / G
gnomAD v3:
8:6883416 A / G
gnomAD v4:
chr8-6883416-A-G
Joint Max Group AF
0.23969085 (AFR)
Genomes Max Group AF
0.23969085 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2738173
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.6883416A>G , CM000670.2:g.6883416A>G
GRCh38
NC_000008.10:g.6740938A>G , CM000670.1:g.6740938A>G
GRCh37
NC_000008.9:g.6728348A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'