ClinGen Allele Registry
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Canonical Allele Identifier:
CA545227162
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.103644217A>G
GRCh37
chr3:g.103363061A>G
Linked Data - Sequence & Population
gnomAD v2:
3:103363061 A / G
gnomAD v3:
3:103644217 A / G
gnomAD v4:
chr3-103644217-A-G
Linked Data - NCBI & NCI
dbSNP:
10937544
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.103644217A>G , CM000665.2:g.103644217A>G
GRCh38
NC_000003.11:g.103363061A>G , CM000665.1:g.103363061A>G
GRCh37
NC_000003.10:g.104845751A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'