ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA158139059
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.45361296C>T
GRCh37
chr7:g.45400895C>T
Linked Data - Sequence & Population
gnomAD v2:
7:45400895 C / T
gnomAD v3:
7:45361296 C / T
gnomAD v4:
chr7-45361296-C-T
Joint Max Group AF
0.60325506 (AFR)
Genomes Max Group AF
0.60325506 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1852612
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.45361296C>T , CM000669.2:g.45361296C>T
GRCh38
NC_000007.13:g.45400895C>T , CM000669.1:g.45400895C>T
GRCh37
NC_000007.12:g.45367420C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'