ClinGen Allele Registry
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Canonical Allele Identifier:
CA12959313
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.78695764A>C
GRCh37
chr9:g.81310680A>C
Linked Data - Sequence & Population
gnomAD v2:
9:81310680 A / C
gnomAD v3:
9:78695764 A / C
gnomAD v4:
chr9-78695764-A-C
Joint Max Group AF
0.38941471 (EAS)
Genomes Max Group AF
0.38941471 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1757948
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.78695764A>C , CM000671.2:g.78695764A>C
GRCh38
NC_000009.11:g.81310680A>C , CM000671.1:g.81310680A>C
GRCh37
NC_000009.10:g.80500500A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'