Canonical Allele Identifier: CA1839197798

Gene: CDKN2B-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22010211_22010212delinsCT , CM000671.2:g.22010211_22010212delinsCT	GRCh38
NC_000009.11:g.22010210_22010211delinsCT , CM000671.1:g.22010210_22010211delinsCT	GRCh37
NC_000009.10:g.22000210_22000211delinsCT	NCBI36
NG_023297.1:g.4102_4103delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-19222_348-19221delinsCT	ENSP00000385916.2:n.348-19222_348-19221delinsCT
ENST00000404796.2:c.348-19222_348-19221delinsCT	ENSP00000385916.2:n.348-19222_348-19221delinsCT
NR_003529.3:n.371+15050_371+15051delinsCT
NR_047532.1:n.371+15050_371+15051delinsCT
NR_047533.1:n.371+15050_371+15051delinsCT
NR_047534.1:n.371+15050_371+15051delinsCT
NR_047535.1:n.371+15050_371+15051delinsCT
NR_047536.1:n.371+15050_371+15051delinsCT
NR_047537.1:n.371+15050_371+15051delinsCT
NR_047538.1:n.371+15050_371+15051delinsCT
NR_047539.1:n.371+15050_371+15051delinsCT
NR_047540.1:n.371+15050_371+15051delinsCT
NR_047541.1:n.371+15050_371+15051delinsCT
NR_047542.1:n.371+15050_371+15051delinsCT
NR_047543.1:n.371+15050_371+15051delinsCT
NR_120536.1:n.371+15050_371+15051delinsCT