ClinGen Allele Registry
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Canonical Allele Identifier:
CA548332330
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.169765063T>C
GRCh37
chr3:g.169482851T>C
Linked Data - Sequence & Population
gnomAD v2:
3:169482851 T / C
gnomAD v3:
3:169765063 T / C
gnomAD v4:
chr3-169765063-T-C
Linked Data - NCBI & NCI
dbSNP:
1246965192
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169765063T>C , CM000665.2:g.169765063T>C
GRCh38
NC_000003.11:g.169482851T>C , CM000665.1:g.169482851T>C
GRCh37
NC_000003.10:g.170965545T>C
NCBI36
NG_016363.1:g.4998A>G , LRG_347:g.4998A>G
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