ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA27681448
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.100718212C>A
GRCh37
chr1:g.101183768C>A
Linked Data - Sequence & Population
gnomAD v3:
1:100718212 C / A
gnomAD v4:
chr1-100718212-C-A
Linked Data - NCBI & NCI
dbSNP:
554936510
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.100718212C>A , CM000663.2:g.100718212C>A
GRCh38
NC_000001.10:g.101183768C>A , CM000663.1:g.101183768C>A
GRCh37
NC_000001.9:g.100956356C>A
NCBI36
NG_023034.2:g.3472C>A
Search 100 bp 5'
Search 100 bp 3'