Canonical Allele Identifier: CA191252962
Gene: CDKN2B-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.22103814A>G
GRCh37 chr9:g.22103813A>G
gnomAD v2:
9:22103813 A / G
gnomAD v3:
9:22103814 A / G
gnomAD v4:
chr9-22103814-A-G
Joint Max Group AF 0.8854082 (AFR)
Genomes Max Group AF 0.8854082 (AFR)
ClinVar Allele:
800887
ClinVar RCV:
RCV001003459
ClinVar Variation:
812641
dbSNP:
1333042
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22103814A>G , CM000671.2:g.22103814A>G GRCh38
NC_000009.11:g.22103813A>G , CM000671.1:g.22103813A>G GRCh37
NC_000009.10:g.22093813A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003529.3:n.2698+6450A>G
NR_047532.1:n.1487+6450A>G
NR_047534.1:n.751+6450A>G
NR_047535.1:n.781-8506A>G
NR_047536.1:n.645-8506A>G
NR_047537.1:n.781-16386A>G
NR_047538.1:n.645-16386A>G
NR_047543.1:n.781-8506A>G
NR_120536.1:n.645-16690A>G
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