ClinGen Allele Registry
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Canonical Allele Identifier:
CA12881628
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.78044423G>A
GRCh37
chr8:g.78956658G>A
Linked Data - Sequence & Population
gnomAD v2:
8:78956658 G / A
gnomAD v3:
8:78044423 G / A
gnomAD v4:
chr8-78044423-G-A
Joint Max Group AF
0.50704552 (SAS)
Genomes Max Group AF
0.50704552 (SAS)
Linked Data - NCBI & NCI
dbSNP:
2219968
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.78044423G>A , CM000670.2:g.78044423G>A
GRCh38
NC_000008.10:g.78956658G>A , CM000670.1:g.78956658G>A
GRCh37
NC_000008.9:g.79119213G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'