ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA14410556
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.74272069A>G
GRCh37
chr17:g.72268208A>G
Linked Data - Sequence & Population
gnomAD v2:
17:72268208 A / G
gnomAD v3:
17:74272069 A / G
gnomAD v4:
chr17-74272069-A-G
Joint Max Group AF
0.97514549 (EAS)
Genomes Max Group AF
0.97514549 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7219585
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.74272069A>G , CM000679.2:g.74272069A>G
GRCh38
NC_000017.10:g.72268208A>G , CM000679.1:g.72268208A>G
GRCh37
NC_000017.9:g.69779803A>G
NCBI36
NG_016865.1:g.2823A>G
Search 100 bp 5'
Search 100 bp 3'