ClinGen Allele Registry
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Canonical Allele Identifier:
CA16448558
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.71938373T>A
GRCh37
chr12:g.72332153T>A
Linked Data - Sequence & Population
gnomAD v2:
12:72332153 T / A
gnomAD v3:
12:71938373 T / A
gnomAD v4:
chr12-71938373-T-A
Joint Max Group AF
0.20786279 (AFR)
Genomes Max Group AF
0.20786279 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11178997
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.71938373T>A , CM000674.2:g.71938373T>A
GRCh38
NC_000012.11:g.72332153T>A , CM000674.1:g.72332153T>A
GRCh37
NC_000012.10:g.70618420T>A
NCBI36
NG_008279.1:g.4528T>A
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