ClinGen Allele Registry
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Canonical Allele Identifier:
CA80429941
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.103172459G>T
GRCh37
chr3:g.102891303G>T
Linked Data - Sequence & Population
gnomAD v2:
3:102891303 G / T
gnomAD v3:
3:103172459 G / T
gnomAD v4:
chr3-103172459-G-T
Joint Max Group AF
0.05251033 (AFR)
Genomes Max Group AF
0.05251033 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6806362
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.103172459G>T , CM000665.2:g.103172459G>T
GRCh38
NC_000003.11:g.102891303G>T , CM000665.1:g.102891303G>T
GRCh37
NC_000003.10:g.104373993G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'