Canonical Allele Identifier: CA15592644
Gene: CDKN2B-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.22103342T>G
GRCh37 chr9:g.22103341T>G
gnomAD v2:
9:22103341 T / G
gnomAD v3:
9:22103342 T / G
gnomAD v4:
chr9-22103342-T-G
Joint Max Group AF 0.88527551 (AFR)
Genomes Max Group AF 0.88527551 (AFR)
ClinVar RCV:
RCV001707229
ClinVar Variation:
1288254
dbSNP:
1537373
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22103342T>G , CM000671.2:g.22103342T>G GRCh38
NC_000009.11:g.22103341T>G , CM000671.1:g.22103341T>G GRCh37
NC_000009.10:g.22093341T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003529.3:n.2698+5978T>G
NR_047532.1:n.1487+5978T>G
NR_047534.1:n.751+5978T>G
NR_047535.1:n.781-8978T>G
NR_047536.1:n.645-8978T>G
NR_047537.1:n.781-16858T>G
NR_047538.1:n.645-16858T>G
NR_047543.1:n.781-8978T>G
NR_120536.1:n.645-17162T>G
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