ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA8070686
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.56960982G>A
GRCh37
chr16:g.56994894G>A
Linked Data - Sequence & Population
gnomAD v2:
16:56994894 G / A
gnomAD v3:
16:56960982 G / A
gnomAD v4:
chr16-56960982-G-A
Joint Max Group AF
0.55520905 (SAS)
Genomes Max Group AF
0.5422856 (SAS)
Exomes Max Group AF
0.55503822 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4783961
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.56960982G>A , CM000678.2:g.56960982G>A
GRCh38
NC_000016.9:g.56994894G>A , CM000678.1:g.56994894G>A
GRCh37
NC_000016.8:g.55552395G>A
NCBI36
NG_008952.1:g.4060G>A
Search 100 bp 5'
Search 100 bp 3'