ClinGen Allele Registry
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Canonical Allele Identifier:
CA196940905
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.101460951C>G
GRCh37
chr9:g.104223233C>G
Linked Data - Sequence & Population
gnomAD v2:
9:104223233 C / G
gnomAD v3:
9:101460951 C / G
gnomAD v4:
chr9-101460951-C-G
Joint Max Group AF
0.81220022 (AFR)
Genomes Max Group AF
0.81220022 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10819937
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.101460951C>G , CM000671.2:g.101460951C>G
GRCh38
NC_000009.11:g.104223233C>G , CM000671.1:g.104223233C>G
GRCh37
NC_000009.10:g.103263054C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'