ClinGen Allele Registry
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Canonical Allele Identifier:
CA855697565
Gene:
Linked Data
dbSNP Id:
rs1464831873
gnomAD v3:
8-79191222-A-G
gnomAD v4:
8-79191222-A-G
MyVariant Identifiers:
chr8:g.80103457A>G (hg19)
chr8:g.79191222A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.79191222A>G , CM000670.2:g.79191222A>G
GRCh38
NC_000008.10:g.80103457A>G , CM000670.1:g.80103457A>G
GRCh37
NC_000008.9:g.80266012A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001745720.1:n.105+851A>G
Search 100 bp 5'
Search 100 bp 3'