Canonical Allele Identifier: CA587092428
Gene: CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1198361636
gnomAD v2: 9-22056607-A-G
gnomAD v3: 9-22056608-A-G
gnomAD v4: 9-22056608-A-G
MyVariant Identifiers: chr9:g.22056607A>G (hg19) chr9:g.22056608A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22056608A>G , CM000671.2:g.22056608A>G GRCh38
NC_000009.11:g.22056607A>G , CM000671.1:g.22056607A>G GRCh37
NC_000009.10:g.22046607A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003529.3:n.1388+221A>G
NR_047532.1:n.1075+221A>G
NR_047533.1:n.644+7380A>G
NR_047534.1:n.644+7380A>G
NR_047535.1:n.780+221A>G
NR_047536.1:n.644+7380A>G
NR_047537.1:n.780+221A>G
NR_047538.1:n.644+7380A>G
NR_047539.1:n.1388+221A>G
NR_047540.1:n.780+221A>G
NR_047541.1:n.780+221A>G
NR_047542.1:n.780+221A>G
NR_047543.1:n.780+221A>G
NR_120536.1:n.644+7380A>G
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