ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA672222006
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.116736721C>G
GRCh37
chr11:g.116607437C>G
Linked Data - NCBI & NCI
dbSNP:
1558861
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.116736721C>G , CM000673.2:g.116736721C>G
GRCh38
NC_000011.9:g.116607437C>G , CM000673.1:g.116607437C>G
GRCh37
NC_000011.8:g.116112647C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'