ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA473651100
Gene:
Linked Data
gnomAD v4:
11-27484081-C-A
MyVariant Identifiers:
chr11:g.27505628C>A (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.27484081C>A , CM000673.2:g.27484081C>A
GRCh38
NC_000011.9:g.27505628C>A , CM000673.1:g.27505628C>A
GRCh37
NC_000011.8:g.27462204C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000496450.1:n.232C>A
Search 100 bp 5'
Search 100 bp 3'