ClinGen Allele Registry
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Canonical Allele Identifier:
CA180022150
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.77266249A>C
GRCh37
chr8:g.78178485A>C
Linked Data - Sequence & Population
gnomAD v2:
8:78178485 A / C
gnomAD v3:
8:77266249 A / C
gnomAD v4:
chr8-77266249-A-C
Joint Max Group AF
0.28316598 (NFE)
Genomes Max Group AF
0.28316598 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6473015
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.77266249A>C , CM000670.2:g.77266249A>C
GRCh38
NC_000008.10:g.78178485A>C , CM000670.1:g.78178485A>C
GRCh37
NC_000008.9:g.78341040A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'