Canonical Allele Identifier: CA862190769

Gene: CDKN2B-AS1

Linked Data

• dbSNP Id: rs1338629533
• gnomAD v3: 9-22000355-ATCTT-A
• gnomAD v4: 9-22000355-ATCTT-A
• MyVariant Identifiers: chr9:g.22000355_22000358del (hg19) ; chr9:g.22000356_22000359del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22000359_22000362del , CM000671.2:g.22000359_22000362del	GRCh38
NC_000009.11:g.22000358_22000361del , CM000671.1:g.22000358_22000361del	GRCh37
NC_000009.10:g.21990358_21990361del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-29074_348-29071del	ENSP00000385916.2:n.348-29074_348-29071del
ENST00000404796.2:c.348-29074_348-29071del	ENSP00000385916.2:n.348-29074_348-29071del
NR_003529.3:n.371+5198_371+5201del
NR_047532.1:n.371+5198_371+5201del
NR_047533.1:n.371+5198_371+5201del
NR_047534.1:n.371+5198_371+5201del
NR_047535.1:n.371+5198_371+5201del
NR_047536.1:n.371+5198_371+5201del
NR_047537.1:n.371+5198_371+5201del
NR_047538.1:n.371+5198_371+5201del
NR_047539.1:n.371+5198_371+5201del
NR_047540.1:n.371+5198_371+5201del
NR_047541.1:n.371+5198_371+5201del
NR_047542.1:n.371+5198_371+5201del
NR_047543.1:n.371+5198_371+5201del
NR_120536.1:n.371+5198_371+5201del