ClinGen Allele Registry
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Canonical Allele Identifier:
CA193640632
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.73543766G>A
GRCh37
chr9:g.76158682G>A
Linked Data - Sequence & Population
gnomAD v2:
9:76158682 G / A
gnomAD v3:
9:73543766 G / A
gnomAD v4:
chr9-73543766-G-A
Joint Max Group AF
0.17307163 (MID)
Genomes Max Group AF
0.16787203 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11143609
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.73543766G>A , CM000671.2:g.73543766G>A
GRCh38
NC_000009.11:g.76158682G>A , CM000671.1:g.76158682G>A
GRCh37
NC_000009.10:g.75348502G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'