ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA584722553
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.116635549G>C
GRCh37
chr8:g.117647788G>C
Linked Data - Sequence & Population
gnomAD v2:
8:117647788 G / C
gnomAD v3:
8:116635549 G / C
gnomAD v4:
chr8-116635549-G-C
Linked Data - NCBI & NCI
dbSNP:
6469656
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.116635549G>C , CM000670.2:g.116635549G>C
GRCh38
NC_000008.10:g.117647788G>C , CM000670.1:g.117647788G>C
GRCh37
NC_000008.9:g.117716969G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'