ClinGen Allele Registry
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Canonical Allele Identifier:
CA13072900
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.105869669G>A
GRCh37
chr9:g.108631950G>A
Linked Data - Sequence & Population
gnomAD v2:
9:108631950 G / A
gnomAD v3:
9:105869669 G / A
gnomAD v4:
chr9-105869669-G-A
Joint Max Group AF
0.5288463 (EAS)
Genomes Max Group AF
0.5288463 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9969729
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.105869669G>A , CM000671.2:g.105869669G>A
GRCh38
NC_000009.11:g.108631950G>A , CM000671.1:g.108631950G>A
GRCh37
NC_000009.10:g.107671771G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'