Canonical Allele Identifier: CA1839197603
Gene: CDKN2B-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22010049_22010053delinsCTTTG , CM000671.2:g.22010049_22010053delinsCTTTG GRCh38
NC_000009.11:g.22010048_22010052delinsCTTTG , CM000671.1:g.22010048_22010052delinsCTTTG GRCh37
NC_000009.10:g.22000048_22000052delinsCTTTG NCBI36
NG_023297.1:g.4261_4265delinsCAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.348-19384_348-19380delinsCTTTG ENSP00000385916.2:n.348-19384_348-19380delinsCTTTG
ENST00000404796.2:c.348-19384_348-19380delinsCTTTG ENSP00000385916.2:n.348-19384_348-19380delinsCTTTG
NR_003529.3:n.371+14888_371+14892delinsCTTTG
NR_047532.1:n.371+14888_371+14892delinsCTTTG
NR_047533.1:n.371+14888_371+14892delinsCTTTG
NR_047534.1:n.371+14888_371+14892delinsCTTTG
NR_047535.1:n.371+14888_371+14892delinsCTTTG
NR_047536.1:n.371+14888_371+14892delinsCTTTG
NR_047537.1:n.371+14888_371+14892delinsCTTTG
NR_047538.1:n.371+14888_371+14892delinsCTTTG
NR_047539.1:n.371+14888_371+14892delinsCTTTG
NR_047540.1:n.371+14888_371+14892delinsCTTTG
NR_047541.1:n.371+14888_371+14892delinsCTTTG
NR_047542.1:n.371+14888_371+14892delinsCTTTG
NR_047543.1:n.371+14888_371+14892delinsCTTTG
NR_120536.1:n.371+14888_371+14892delinsCTTTG