ClinGen Allele Registry
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Canonical Allele Identifier:
CA146503198
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.118332041G>C
GRCh37
chr6:g.118653204G>C
Linked Data - Sequence & Population
gnomAD v2:
6:118653204 G / C
gnomAD v3:
6:118332041 G / C
gnomAD v4:
chr6-118332041-G-C
Joint Max Group AF
0.06552916 (SAS)
Genomes Max Group AF
0.06552916 (SAS)
Linked Data - NCBI & NCI
dbSNP:
12210810
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.118332041G>C , CM000668.2:g.118332041G>C
GRCh38
NC_000006.11:g.118653204G>C , CM000668.1:g.118653204G>C
GRCh37
NC_000006.10:g.118759897G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'