ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15749349
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.91133404A>G
GRCh37
chr12:g.91527181A>G
Linked Data - Sequence & Population
gnomAD v2:
12:91527181 A / G
gnomAD v3:
12:91133404 A / G
gnomAD v4:
chr12-91133404-A-G
Joint Max Group AF
0.58475273 (AFR)
Genomes Max Group AF
0.58475273 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7308752
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.91133404A>G , CM000674.2:g.91133404A>G
GRCh38
NC_000012.11:g.91527181A>G , CM000674.1:g.91527181A>G
GRCh37
NC_000012.10:g.90051312A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'