ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13623474
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.63154939T>A
GRCh37
chr12:g.63548719T>A
Linked Data - Sequence & Population
gnomAD v2:
12:63548719 T / A
gnomAD v3:
12:63154939 T / A
gnomAD v4:
chr12-63154939-T-A
Joint Max Group AF
0.52319034 (AFR)
Genomes Max Group AF
0.52319034 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7298346
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.63154939T>A , CM000674.2:g.63154939T>A
GRCh38
NC_000012.11:g.63548719T>A , CM000674.1:g.63548719T>A
GRCh37
NC_000012.10:g.61834986T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'