ClinGen Allele Registry
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Canonical Allele Identifier:
CA844535564
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.99995723C>G
GRCh37
chr7:g.99593346C>G
Linked Data - Sequence & Population
gnomAD v3:
7:99995723 C / G
gnomAD v4:
chr7-99995723-C-G
Linked Data - NCBI & NCI
dbSNP:
4727443
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.99995723C>G , CM000669.2:g.99995723C>G
GRCh38
NC_000007.13:g.99593346C>G , CM000669.1:g.99593346C>G
GRCh37
NC_000007.12:g.99431282C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'