ClinGen Allele Registry
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Canonical Allele Identifier:
CA198905218
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114842790T>C
GRCh37
chr9:g.117605070T>C
Linked Data - Sequence & Population
gnomAD v2:
9:117605070 T / C
gnomAD v3:
9:114842790 T / C
gnomAD v4:
chr9-114842790-T-C
Joint Max Group AF
0.19986932 (SAS)
Genomes Max Group AF
0.19986932 (SAS)
Linked Data - NCBI & NCI
dbSNP:
11554257
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114842790T>C , CM000671.2:g.114842790T>C
GRCh38
NC_000009.11:g.117605070T>C , CM000671.1:g.117605070T>C
GRCh37
NC_000009.10:g.116644891T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'