Canonical Allele Identifier: CA191246635
Gene: CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs998149795
gnomAD v2: 9-22056362-C-T
gnomAD v3: 9-22056363-C-T
gnomAD v4: 9-22056363-C-T
MyVariant Identifiers: chr9:g.22056362C>T (hg19) chr9:g.22056363C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22056363C>T , CM000671.2:g.22056363C>T GRCh38
NC_000009.11:g.22056362C>T , CM000671.1:g.22056362C>T GRCh37
NC_000009.10:g.22046362C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003529.3:n.1364C>T
NR_047532.1:n.1051C>T
NR_047533.1:n.644+7135C>T
NR_047534.1:n.644+7135C>T
NR_047535.1:n.756C>T
NR_047536.1:n.644+7135C>T
NR_047537.1:n.756C>T
NR_047538.1:n.644+7135C>T
NR_047539.1:n.1364C>T
NR_047540.1:n.756C>T
NR_047541.1:n.756C>T
NR_047542.1:n.756C>T
NR_047543.1:n.756C>T
NR_120536.1:n.644+7135C>T
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