ClinGen Allele Registry
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Canonical Allele Identifier:
CA900278338
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.1470903C>T
GRCh37
chr3:g.1512587C>T
Linked Data - Sequence & Population
gnomAD v3:
3:1470903 C / T
gnomAD v4:
chr3-1470903-C-T
Linked Data - NCBI & NCI
dbSNP:
6763848
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.1470903C>T , CM000665.2:g.1470903C>T
GRCh38
NC_000003.11:g.1512587C>T , CM000665.1:g.1512587C>T
GRCh37
NC_000003.10:g.1487587C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'