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Canonical Allele Identifier:
CA13677233
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.120965129C>T
GRCh37
chr12:g.121402932C>T
Linked Data - Sequence & Population
gnomAD v2:
12:121402932 C / T
gnomAD v3:
12:120965129 C / T
gnomAD v4:
chr12-120965129-C-T
Joint Max Group AF
0.5160318 (EAS)
Genomes Max Group AF
0.5160318 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7305618
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.120965129C>T , CM000674.2:g.120965129C>T
GRCh38
NC_000012.11:g.121402932C>T , CM000674.1:g.121402932C>T
GRCh37
NC_000012.10:g.119887315C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'