ClinGen Allele Registry
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Canonical Allele Identifier:
CA12266566
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32696681T>C
GRCh37
chr6:g.32664458T>C
Linked Data - Sequence & Population
gnomAD v2:
6:32664458 T / C
gnomAD v3:
6:32696681 T / C
gnomAD v4:
chr6-32696681-T-C
Joint Max Group AF
0.79739402 (EAS)
Genomes Max Group AF
0.79739402 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2647012
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32696681T>C , CM000668.2:g.32696681T>C
GRCh38
NC_000006.11:g.32664458T>C , CM000668.1:g.32664458T>C
GRCh37
NC_000006.10:g.32772436T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'