Canonical Allele Identifier: CA1122171139

Gene: CDKN2B-AS1

Linked Data

• dbSNP Id: rs1821426248
• gnomAD v3: 9-22010152-AAG-A
• gnomAD v4: 9-22010152-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22010157_22010158del , CM000671.2:g.22010157_22010158del	GRCh38
NC_000009.11:g.22010156_22010157del , CM000671.1:g.22010156_22010157del	GRCh37
NC_000009.10:g.22000156_22000157del	NCBI36
NG_023297.1:g.4160_4161del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-19276_348-19275del	ENSP00000385916.2:n.348-19276_348-19275del
ENST00000404796.2:c.348-19276_348-19275del	ENSP00000385916.2:n.348-19276_348-19275del
NR_003529.3:n.371+14996_371+14997del
NR_047532.1:n.371+14996_371+14997del
NR_047533.1:n.371+14996_371+14997del
NR_047534.1:n.371+14996_371+14997del
NR_047535.1:n.371+14996_371+14997del
NR_047536.1:n.371+14996_371+14997del
NR_047537.1:n.371+14996_371+14997del
NR_047538.1:n.371+14996_371+14997del
NR_047539.1:n.371+14996_371+14997del
NR_047540.1:n.371+14996_371+14997del
NR_047541.1:n.371+14996_371+14997del
NR_047542.1:n.371+14996_371+14997del
NR_047543.1:n.371+14996_371+14997del
NR_120536.1:n.371+14996_371+14997del