ClinGen Allele Registry
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Canonical Allele Identifier:
CA13760299
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.17487017T>A
GRCh37
chr12:g.17639951T>A
Linked Data - Sequence & Population
gnomAD v2:
12:17639951 T / A
gnomAD v3:
12:17487017 T / A
gnomAD v4:
chr12-17487017-T-A
Joint Max Group AF
0.59773279 (SAS)
Genomes Max Group AF
0.59773279 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10219673
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.17487017T>A , CM000674.2:g.17487017T>A
GRCh38
NC_000012.11:g.17639951T>A , CM000674.1:g.17639951T>A
GRCh37
NC_000012.10:g.17531218T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'