ClinGen Allele Registry
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Canonical Allele Identifier:
CA155920047
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.26143126C>A
GRCh37
chr7:g.26182746C>A
Linked Data - Sequence & Population
gnomAD v2:
7:26182746 C / A
gnomAD v3:
7:26143126 C / A
gnomAD v4:
chr7-26143126-C-A
Joint Max Group AF
0.03531445 (NFE)
Genomes Max Group AF
0.03531445 (NFE)
Linked Data - NCBI & NCI
dbSNP:
73279689
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.26143126C>A , CM000669.2:g.26143126C>A
GRCh38
NC_000007.13:g.26182746C>A , CM000669.1:g.26182746C>A
GRCh37
NC_000007.12:g.26149271C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'