ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12966764
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.106836765G>A
GRCh37
chr9:g.109599046G>A
Linked Data - Sequence & Population
gnomAD v2:
9:109599046 G / A
gnomAD v3:
9:106836765 G / A
gnomAD v4:
chr9-106836765-G-A
Joint Max Group AF
0.24799429 (SAS)
Genomes Max Group AF
0.24799429 (SAS)
Linked Data - NCBI & NCI
dbSNP:
7027110
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.106836765G>A , CM000671.2:g.106836765G>A
GRCh38
NC_000009.11:g.109599046G>A , CM000671.1:g.109599046G>A
GRCh37
NC_000009.10:g.108638867G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'