ClinGen Allele Registry
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Canonical Allele Identifier:
CA15067051
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.121787363C>A
GRCh37
chr9:g.124549642C>A
Linked Data - Sequence & Population
gnomAD v2:
9:124549642 C / A
gnomAD v3:
9:121787363 C / A
gnomAD v4:
chr9-121787363-C-A
Joint Max Group AF
0.20258854 (EAS)
Genomes Max Group AF
0.20258854 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10985375
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.121787363C>A , CM000671.2:g.121787363C>A
GRCh38
NC_000009.11:g.124549642C>A , CM000671.1:g.124549642C>A
GRCh37
NC_000009.10:g.123589463C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'