ClinGen Allele Registry
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Canonical Allele Identifier:
CA12585298
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.35567623G>A
GRCh37
chr7:g.35607233G>A
Linked Data - Sequence & Population
gnomAD v2:
7:35607233 G / A
gnomAD v3:
7:35567623 G / A
gnomAD v4:
chr7-35567623-G-A
Joint Max Group AF
0.72218695 (EAS)
Genomes Max Group AF
0.72218695 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6973609
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.35567623G>A , CM000669.2:g.35567623G>A
GRCh38
NC_000007.13:g.35607233G>A , CM000669.1:g.35607233G>A
GRCh37
NC_000007.12:g.35573758G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'