Canonical Allele Identifier: CA1839193236
Gene: CDKN2B HGNC NCBI
CDKN2B-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22006261_22006263delinsCAG , CM000671.2:g.22006261_22006263delinsCAG GRCh38
NC_000009.11:g.22006260_22006262delinsCAG , CM000671.1:g.22006260_22006262delinsCAG GRCh37
NC_000009.10:g.21996260_21996262delinsCAG NCBI36
NG_023297.1:g.8051_8053delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000276925.7:c.157-16_157-14delinsCTG (CDKN2B) MANE Select ENSP00000276925.6:n.157-16_157-14delinsCT...
ENST00000380142.5:c.*43-16_*43-14delinsCTG (CDKN2B) ENSP00000369487.4:n.*43-16_*43-14delinsCT...
ENST00000404796.3:c.348-23172_348-23170delinsCAG ENSP00000385916.2:n.348-23172_348-23170de...
ENST00000276925.6:c.157-16_157-14delinsCTG (CDKN2B) ENSP00000276925.6:n.157-16_157-14delinsCT...
ENST00000380142.4:c.*43-16_*43-14delinsCTG (CDKN2B) ENSP00000369487.4:n.*43-16_*43-14delinsCT...
ENST00000404796.2:c.348-23172_348-23170delinsCAG ENSP00000385916.2:n.348-23172_348-23170de...
ENST00000579591.1:n.9_11delinsCTG (CDKN2B)
NM_004936.3:c.157-16_157-14delinsCTG (CDKN2B) NP_004927.2:n.157-16_157-14delinsCTG
NM_078487.2:c.*43-16_*43-14delinsCTG (CDKN2B) NP_511042.1:n.*43-16_*43-14delinsCTG
NR_003529.3:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047532.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047533.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047534.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047535.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047536.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047537.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047538.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047539.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047540.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047541.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047542.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_047543.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NR_120536.1:n.371+11100_371+11102delinsCAG (CDKN2B-AS1)
NM_004936.4:c.157-16_157-14delinsCTG (CDKN2B) MANE Select NP_004927.2:n.157-16_157-14delinsCTG