ClinGen Allele Registry
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Canonical Allele Identifier:
CA13677234
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.120965921G>A
GRCh37
chr12:g.121403724G>A
Linked Data - Sequence & Population
gnomAD v2:
12:121403724 G / A
gnomAD v3:
12:120965921 G / A
gnomAD v4:
chr12-120965921-G-A
Joint Max Group AF
0.64934635 (AFR)
Genomes Max Group AF
0.64935451 (AFR)
Exomes Max Group AF
0.33098066 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7953249
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.120965921G>A , CM000674.2:g.120965921G>A
GRCh38
NC_000012.11:g.121403724G>A , CM000674.1:g.121403724G>A
GRCh37
NC_000012.10:g.119888107G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'