ClinGen Allele Registry
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Canonical Allele Identifier:
CA562052923
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.110854370A>G
GRCh37
chr5:g.110190069A>G
Linked Data - Sequence & Population
gnomAD v2:
5:110190069 A / G
gnomAD v3:
5:110854370 A / G
gnomAD v4:
chr5-110854370-A-G
Linked Data - NCBI & NCI
dbSNP:
1407639455
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.110854370A>G , CM000667.2:g.110854370A>G
GRCh38
NC_000005.9:g.110190069A>G , CM000667.1:g.110190069A>G
GRCh37
NC_000005.8:g.110217968A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'