ClinGen Allele Registry
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Canonical Allele Identifier:
CA15611220
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.117699343C>T
GRCh37
chr9:g.120461621C>T
Linked Data - Sequence & Population
gnomAD v2:
9:120461621 C / T
gnomAD v3:
9:117699343 C / T
gnomAD v4:
chr9-117699343-C-T
Joint Max Group AF
0.59818091 (EAS)
Genomes Max Group AF
0.59818091 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10759930
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.117699343C>T , CM000671.2:g.117699343C>T
GRCh38
NC_000009.11:g.120461621C>T , CM000671.1:g.120461621C>T
GRCh37
NC_000009.10:g.119501442C>T
NCBI36
NG_011475.1:g.162C>T
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