ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13110599
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.105892815G>T
GRCh37
chr9:g.108655096G>T
Linked Data - Sequence & Population
gnomAD v2:
9:108655096 G / T
gnomAD v3:
9:105892815 G / T
gnomAD v4:
chr9-105892815-G-T
Joint Max Group AF
0.49345929 (EAS)
Genomes Max Group AF
0.49345929 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4742971
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.105892815G>T , CM000671.2:g.105892815G>T
GRCh38
NC_000009.11:g.108655096G>T , CM000671.1:g.108655096G>T
GRCh37
NC_000009.10:g.107694917G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'