ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA747163363
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.14472675A>G
GRCh37
chr21:g.15844996A>G
Linked Data - NCBI & NCI
dbSNP:
1329751313
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.14472675A>G , CM000683.2:g.14472675A>G
GRCh38
NC_000021.8:g.15844996A>G , CM000683.1:g.15844996A>G
GRCh37
NC_000021.7:g.14766867A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'