ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA902378607
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.169765328C>A
GRCh37
chr3:g.169483116C>A
Linked Data - Sequence & Population
gnomAD v3:
3:169765328 C / A
gnomAD v4:
chr3-169765328-C-A
Linked Data - NCBI & NCI
dbSNP:
1459634628
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169765328C>A , CM000665.2:g.169765328C>A
GRCh38
NC_000003.11:g.169483116C>A , CM000665.1:g.169483116C>A
GRCh37
NC_000003.10:g.170965810C>A
NCBI36
NG_016363.1:g.4733G>T , LRG_347:g.4733G>T
Search 100 bp 5'
Search 100 bp 3'