ClinGen Allele Registry
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Canonical Allele Identifier:
CA13759897
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.13379397G>C
GRCh37
chr12:g.13532331G>C
Linked Data - Sequence & Population
gnomAD v2:
12:13532331 G / C
gnomAD v3:
12:13379397 G / C
gnomAD v4:
chr12-13379397-G-C
Joint Max Group AF
0.48239306 (AMR)
Genomes Max Group AF
0.48239306 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1993508
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.13379397G>C , CM000674.2:g.13379397G>C
GRCh38
NC_000012.11:g.13532331G>C , CM000674.1:g.13532331G>C
GRCh37
NC_000012.10:g.13423598G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'