Canonical Allele Identifier: CA13104891
Gene: CDKN2B HGNC NCBI
CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs3217989
gnomAD v2: 9-22003790-T-C
gnomAD v3: 9-22003791-T-C
gnomAD v4: 9-22003791-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22003791T>C , CM000671.2:g.22003791T>C GRCh38
NC_000009.11:g.22003790T>C , CM000671.1:g.22003790T>C GRCh37
NC_000009.10:g.21993790T>C NCBI36
NG_023297.1:g.10523A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000276925.7:c.*2196A>G (CDKN2B) MANE Select ENSP00000276925.6:n.*2196A>G
ENST00000404796.3:c.348-25642T>C ENSP00000385916.2:n.348-25642T>C
ENST00000276925.6:c.*2196A>G (CDKN2B) ENSP00000276925.6:n.*2196A>G
ENST00000404796.2:c.348-25642T>C ENSP00000385916.2:n.348-25642T>C
NM_004936.3:c.*2196A>G (CDKN2B) NP_004927.2:n.*2196A>G
NM_078487.2:c.*2499A>G (CDKN2B) NP_511042.1:n.*2499A>G
NR_003529.3:n.371+8630T>C (CDKN2B-AS1)
NR_047532.1:n.371+8630T>C (CDKN2B-AS1)
NR_047533.1:n.371+8630T>C (CDKN2B-AS1)
NR_047534.1:n.371+8630T>C (CDKN2B-AS1)
NR_047535.1:n.371+8630T>C (CDKN2B-AS1)
NR_047536.1:n.371+8630T>C (CDKN2B-AS1)
NR_047537.1:n.371+8630T>C (CDKN2B-AS1)
NR_047538.1:n.371+8630T>C (CDKN2B-AS1)
NR_047539.1:n.371+8630T>C (CDKN2B-AS1)
NR_047540.1:n.371+8630T>C (CDKN2B-AS1)
NR_047541.1:n.371+8630T>C (CDKN2B-AS1)
NR_047542.1:n.371+8630T>C (CDKN2B-AS1)
NR_047543.1:n.371+8630T>C (CDKN2B-AS1)
NR_120536.1:n.371+8630T>C (CDKN2B-AS1)
NM_004936.4:c.*2196A>G (CDKN2B) MANE Select NP_004927.2:n.*2196A>G