Canonical Allele Identifier: CA5012527
Gene: CDKN2B HGNC NCBI
CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs771295942
ExAC: 9:22006258 A / G
gnomAD v2: 9-22006258-A-G
gnomAD v3: 9-22006259-A-G
gnomAD v4: 9-22006259-A-G
MyVariant Identifiers: chr9:g.22006258A>G (hg19) chr9:g.22006259A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22006259A>G , CM000671.2:g.22006259A>G GRCh38
NC_000009.11:g.22006258A>G , CM000671.1:g.22006258A>G GRCh37
NC_000009.10:g.21996258A>G NCBI36
NG_023297.1:g.8055T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000276925.7:c.157-12T>C (CDKN2B) MANE Select ENSP00000276925.6:n.157-12T>C
ENST00000380142.5:c.*43-12T>C (CDKN2B) ENSP00000369487.4:n.*43-12T>C
ENST00000404796.3:c.348-23174A>G ENSP00000385916.2:n.348-23174A>G
ENST00000276925.6:c.157-12T>C (CDKN2B) ENSP00000276925.6:n.157-12T>C
ENST00000380142.4:c.*43-12T>C (CDKN2B) ENSP00000369487.4:n.*43-12T>C
ENST00000404796.2:c.348-23174A>G ENSP00000385916.2:n.348-23174A>G
ENST00000579591.1:n.13T>C (CDKN2B)
NM_004936.3:c.157-12T>C (CDKN2B) NP_004927.2:n.157-12T>C
NM_078487.2:c.*43-12T>C (CDKN2B) NP_511042.1:n.*43-12T>C
NR_003529.3:n.371+11098A>G (CDKN2B-AS1)
NR_047532.1:n.371+11098A>G (CDKN2B-AS1)
NR_047533.1:n.371+11098A>G (CDKN2B-AS1)
NR_047534.1:n.371+11098A>G (CDKN2B-AS1)
NR_047535.1:n.371+11098A>G (CDKN2B-AS1)
NR_047536.1:n.371+11098A>G (CDKN2B-AS1)
NR_047537.1:n.371+11098A>G (CDKN2B-AS1)
NR_047538.1:n.371+11098A>G (CDKN2B-AS1)
NR_047539.1:n.371+11098A>G (CDKN2B-AS1)
NR_047540.1:n.371+11098A>G (CDKN2B-AS1)
NR_047541.1:n.371+11098A>G (CDKN2B-AS1)
NR_047542.1:n.371+11098A>G (CDKN2B-AS1)
NR_047543.1:n.371+11098A>G (CDKN2B-AS1)
NR_120536.1:n.371+11098A>G (CDKN2B-AS1)
NM_004936.4:c.157-12T>C (CDKN2B) MANE Select NP_004927.2:n.157-12T>C
Search 100 bp 5'
Search 100 bp 3'