ClinGen Allele Registry
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Canonical Allele Identifier:
CA439480767
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.55547195C>G
GRCh37
chr4:g.56413362C>G
Linked Data - Sequence & Population
gnomAD v2:
4:56413362 C / G
gnomAD v3:
4:55547195 C / G
gnomAD v4:
chr4-55547195-C-G
Linked Data - NCBI & NCI
dbSNP:
192518038
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.55547195C>G , CM000666.2:g.55547195C>G
GRCh38
NC_000004.11:g.56413362C>G , CM000666.1:g.56413362C>G
GRCh37
NC_000004.10:g.56108119C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'