ClinGen Allele Registry
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Canonical Allele Identifier:
CA15086576
Gene: PKN2-AS1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.88677622C>T
GRCh37
chr1:g.89143305C>T
Linked Data - Sequence & Population
gnomAD v2:
1:89143305 C / T
gnomAD v3:
1:88677622 C / T
gnomAD v4:
chr1-88677622-C-T
Joint Max Group AF
0.37675667 (AMR)
Genomes Max Group AF
0.37675667 (AMR)
Linked Data - NCBI & NCI
dbSNP:
6698181
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.88677622C>T , CM000663.2:g.88677622C>T
GRCh38
NC_000001.10:g.89143305C>T , CM000663.1:g.89143305C>T
GRCh37
NC_000001.9:g.88915893C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_110682.1:n.41+7542G>A
Search 100 bp 5'
Search 100 bp 3'