Canonical Allele Identifier: CA190750487

Gene: CDKN2B CDKN2B-AS1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22005141_22005142insTG , CM000671.2:g.22005141_22005142insTG	GRCh38
NC_000009.11:g.22005140_22005141insTG , CM000671.1:g.22005140_22005141insTG	GRCh37
NC_000009.10:g.21995140_21995141insTG	NCBI36
NG_023297.1:g.9172_9173insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276925.7:c.*845_*846insCA (CDKN2B) MANE Select	ENSP00000276925.6:n.*845_*846insCA
ENST00000380142.5:c.*1148_*1149insCA (CDKN2B)	ENSP00000369487.4:n.*1148_*1149insCA
ENST00000404796.3:c.348-24292_348-24291insTG	ENSP00000385916.2:n.348-24292_348-24291insTG
ENST00000276925.6:c.*845_*846insCA (CDKN2B)	ENSP00000276925.6:n.*845_*846insCA
ENST00000404796.2:c.348-24292_348-24291insTG	ENSP00000385916.2:n.348-24292_348-24291insTG
NM_004936.3:c.*845_*846insCA (CDKN2B)	NP_004927.2:n.*845_*846insCA
NM_078487.2:c.*1148_*1149insCA (CDKN2B)	NP_511042.1:n.*1148_*1149insCA
NR_003529.3:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047532.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047533.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047534.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047535.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047536.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047537.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047538.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047539.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047540.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047541.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047542.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_047543.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NR_120536.1:n.371+9980_371+9981insTG (CDKN2B-AS1)
NM_004936.4:c.*845_*846insCA (CDKN2B) MANE Select	NP_004927.2:n.*845_*846insCA