ClinGen Allele Registry
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Canonical Allele Identifier:
CA903941322
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.186841685C>T
GRCh37
chr3:g.186559474C>T
Linked Data - Sequence & Population
gnomAD v3:
3:186841685 C / T
gnomAD v4:
chr3-186841685-C-T
Linked Data - NCBI & NCI
dbSNP:
266729
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.186841685C>T , CM000665.2:g.186841685C>T
GRCh38
NC_000003.11:g.186559474C>T , CM000665.1:g.186559474C>T
GRCh37
NC_000003.10:g.188042168C>T
NCBI36
NG_021140.1:g.4012C>T
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