ClinGen Allele Registry
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Canonical Allele Identifier:
CA198901287
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114806789G>C
GRCh37
chr9:g.117569069G>C
Linked Data - Sequence & Population
gnomAD v3:
9:114806789 G / C
gnomAD v4:
chr9-114806789-G-C
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
971338129
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114806789G>C , CM000671.2:g.114806789G>C
GRCh38
NC_000009.11:g.117569069G>C , CM000671.1:g.117569069G>C
GRCh37
NC_000009.10:g.116608890G>C
NCBI36
NG_011488.2:g.4340C>G
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