ClinGen Allele Registry
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Canonical Allele Identifier:
CA13699870
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.130146390T>C
GRCh37
chr12:g.130630935T>C
Linked Data - Sequence & Population
gnomAD v2:
12:130630935 T / C
gnomAD v3:
12:130146390 T / C
gnomAD v4:
chr12-130146390-T-C
Joint Max Group AF
0.19617668 (EAS)
Genomes Max Group AF
0.19617668 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11060736
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.130146390T>C , CM000674.2:g.130146390T>C
GRCh38
NC_000012.11:g.130630935T>C , CM000674.1:g.130630935T>C
GRCh37
NC_000012.10:g.129196888T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'