ClinGen Allele Registry
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Canonical Allele Identifier:
CA547937236
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.169765315A>G
GRCh37
chr3:g.169483103A>G
Linked Data - Sequence & Population
gnomAD v2:
3:169483103 A / G
gnomAD v3:
3:169765315 A / G
gnomAD v4:
chr3-169765315-A-G
Linked Data - NCBI & NCI
dbSNP:
1387582408
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169765315A>G , CM000665.2:g.169765315A>G
GRCh38
NC_000003.11:g.169483103A>G , CM000665.1:g.169483103A>G
GRCh37
NC_000003.10:g.170965797A>G
NCBI36
NG_016363.1:g.4746T>C , LRG_347:g.4746T>C
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