ClinGen Allele Registry
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Canonical Allele Identifier:
CA294733352
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.78925567G>A
GRCh37
chr17:g.76921649G>A
Linked Data - Sequence & Population
gnomAD v2:
17:76921649 G / A
gnomAD v3:
17:78925567 G / A
gnomAD v4:
chr17-78925567-G-A
Joint Max Group AF
0.19510451 (SAS)
Genomes Max Group AF
0.19510451 (SAS)
Linked Data - NCBI & NCI
dbSNP:
8179096
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.78925567G>A , CM000679.2:g.78925567G>A
GRCh38
NC_000017.10:g.76921649G>A , CM000679.1:g.76921649G>A
GRCh37
NC_000017.9:g.74433244G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'