ClinGen Allele Registry
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Canonical Allele Identifier:
CA11442655
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.47347457T>A
GRCh37
chr3:g.47388947T>A
Linked Data - Sequence & Population
gnomAD v2:
3:47388947 T / A
gnomAD v3:
3:47347457 T / A
gnomAD v4:
chr3-47347457-T-A
Joint Max Group AF
0.43813016 (AMR)
Genomes Max Group AF
0.43813016 (AMR)
Linked Data - NCBI & NCI
dbSNP:
8180040
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.47347457T>A , CM000665.2:g.47347457T>A
GRCh38
NC_000003.11:g.47388947T>A , CM000665.1:g.47388947T>A
GRCh37
NC_000003.10:g.47363951T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'