ClinGen Allele Registry
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Canonical Allele Identifier:
CA13613154
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.8552873T>A
GRCh37
chr12:g.8705469T>A
Linked Data - Sequence & Population
gnomAD v2:
12:8705469 T / A
gnomAD v3:
12:8552873 T / A
gnomAD v4:
chr12-8552873-T-A
Joint Max Group AF
0.61307798 (EAS)
Genomes Max Group AF
0.61307798 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10770857
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.8552873T>A , CM000674.2:g.8552873T>A
GRCh38
NC_000012.11:g.8705469T>A , CM000674.1:g.8705469T>A
GRCh37
NC_000012.10:g.8596736T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'