ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA73374881
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.36638607G>T
GRCh37
chr3:g.36680099G>T
Linked Data - Sequence & Population
gnomAD v2:
3:36680099 G / T
gnomAD v3:
3:36638607 G / T
gnomAD v4:
chr3-36638607-G-T
Joint Max Group AF
0.54306173 (AMR)
Genomes Max Group AF
0.54306173 (AMR)
Linked Data - NCBI & NCI
dbSNP:
950146
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.36638607G>T , CM000665.2:g.36638607G>T
GRCh38
NC_000003.11:g.36680099G>T , CM000665.1:g.36680099G>T
GRCh37
NC_000003.10:g.36655103G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'