Canonical Allele Identifier: CA587093498

Gene: CDKN2B-AS1

Linked Data

• dbSNP Id: rs1304756840
• gnomAD v2: 9-22061287-CTTTTCCTTTACTAGCCAAAATCTGATGACATT-C
• gnomAD v3: 9-22061288-CTTTTCCTTTACTAGCCAAAATCTGATGACATT-C
• gnomAD v4: 9-22061288-CTTTTCCTTTACTAGCCAAAATCTGATGACATT-C
• MyVariant Identifiers: chr9:g.22061288_22061319del (hg19) ; chr9:g.22061289_22061320del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22061309_22061340del , CM000671.2:g.22061309_22061340del	GRCh38
NC_000009.11:g.22061308_22061339del , CM000671.1:g.22061308_22061339del	GRCh37
NC_000009.10:g.22051308_22051339del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003529.3:n.2085-644_2085-613del
NR_047532.1:n.1075+4922_1075+4953del
NR_047533.1:n.644+12081_644+12112del
NR_047534.1:n.644+12081_644+12112del
NR_047535.1:n.780+4922_780+4953del
NR_047536.1:n.644+12081_644+12112del
NR_047537.1:n.780+4922_780+4953del
NR_047538.1:n.644+12081_644+12112del
NR_047539.1:n.2085-644_2085-613del
NR_047540.1:n.781-644_781-613del
NR_047541.1:n.781-2635_781-2604del
NR_047542.1:n.780+4922_780+4953del
NR_047543.1:n.780+4922_780+4953del
NR_120536.1:n.644+12081_644+12112del