ClinGen Allele Registry
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Canonical Allele Identifier:
CA191256914
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.22134030G>A
GRCh37
chr9:g.22134029G>A
Linked Data - Sequence & Population
gnomAD v2:
9:22134029 G / A
gnomAD v3:
9:22134030 G / A
gnomAD v4:
chr9-22134030-G-A
Joint Max Group AF
0.06891834 (EAS)
Genomes Max Group AF
0.06891834 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10965251
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.22134030G>A , CM000671.2:g.22134030G>A
GRCh38
NC_000009.11:g.22134029G>A , CM000671.1:g.22134029G>A
GRCh37
NC_000009.10:g.22124029G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'