ClinGen Allele Registry
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Canonical Allele Identifier:
CA11427612
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.169747154C>T
GRCh37
chr3:g.169464942C>T
Linked Data - Sequence & Population
gnomAD v2:
3:169464942 C / T
gnomAD v3:
3:169747154 C / T
gnomAD v4:
chr3-169747154-C-T
Joint Max Group AF
0.45761334 (EAS)
Genomes Max Group AF
0.45761334 (EAS)
Linked Data - NCBI & NCI
dbSNP:
13097028
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169747154C>T , CM000665.2:g.169747154C>T
GRCh38
NC_000003.11:g.169464942C>T , CM000665.1:g.169464942C>T
GRCh37
NC_000003.10:g.170947636C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'