ClinGen Allele Registry
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Canonical Allele Identifier:
CA11479051
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.103731747A>C
GRCh37
chr3:g.103450591A>C
Linked Data - Sequence & Population
gnomAD v2:
3:103450591 A / C
gnomAD v3:
3:103731747 A / C
gnomAD v4:
chr3-103731747-A-C
Joint Max Group AF
0.61006895 (NFE)
Genomes Max Group AF
0.61006895 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2677247
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.103731747A>C , CM000665.2:g.103731747A>C
GRCh38
NC_000003.11:g.103450591A>C , CM000665.1:g.103450591A>C
GRCh37
NC_000003.10:g.104933281A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'