Canonical Allele Identifier: CA191250708
Gene: CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs996259133
gnomAD v3: 9-22088116-GCT-G
gnomAD v4: 9-22088116-GCT-G
MyVariant Identifiers: chr9:g.22088116_22088117del (hg19) chr9:g.22088117_22088118del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22088119_22088120del , CM000671.2:g.22088119_22088120del GRCh38
NC_000009.11:g.22088118_22088119del , CM000671.1:g.22088118_22088119del GRCh37
NC_000009.10:g.22078118_22078119del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003529.3:n.2449-8253_2449-8252del
NR_047532.1:n.1076-4189_1076-4188del
NR_047534.1:n.645-9139_645-9138del
NR_047535.1:n.781-24201_781-24200del
NR_047536.1:n.645-24201_645-24200del
NR_047537.1:n.780+31732_780+31733del
NR_047538.1:n.645-32081_645-32080del
NR_047543.1:n.781-24201_781-24200del
NR_120536.1:n.645-32385_645-32384del
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