ClinGen Allele Registry
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Canonical Allele Identifier:
CA121718406
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.79517086A>G
GRCh37
chr5:g.78812909A>G
Linked Data - Sequence & Population
gnomAD v2:
5:78812909 A / G
gnomAD v3:
5:79517086 A / G
gnomAD v4:
chr5-79517086-A-G
Joint Max Group AF
0.25886376 (AFR)
Genomes Max Group AF
0.25886376 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4704559
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.79517086A>G , CM000667.2:g.79517086A>G
GRCh38
NC_000005.9:g.78812909A>G , CM000667.1:g.78812909A>G
GRCh37
NC_000005.8:g.78848665A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'