ClinGen Allele Registry
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Canonical Allele Identifier:
CA14456159
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.34266955G>A
GRCh37
chr17:g.32593974G>A
Linked Data - Sequence & Population
gnomAD v2:
17:32593974 G / A
gnomAD v3:
17:34266955 G / A
gnomAD v4:
chr17-34266955-G-A
Joint Max Group AF
0.53905375 (EAS)
Genomes Max Group AF
0.53905375 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3091316
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.34266955G>A , CM000679.2:g.34266955G>A
GRCh38
NC_000017.10:g.32593974G>A , CM000679.1:g.32593974G>A
GRCh37
NC_000017.9:g.29618087G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'