Canonical Allele Identifier: CA190748703

Gene: CDKN2B-AS1

Linked Data

• dbSNP Id: rs1048803089
• gnomAD v3: 9-22000426-TCTAA-T
• gnomAD v4: 9-22000426-TCTAA-T
• MyVariant Identifiers: chr9:g.22000426_22000429del (hg19) ; chr9:g.22000427_22000430del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22000430_22000433del , CM000671.2:g.22000430_22000433del	GRCh38
NC_000009.11:g.22000429_22000432del , CM000671.1:g.22000429_22000432del	GRCh37
NC_000009.10:g.21990429_21990432del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-29003_348-29000del	ENSP00000385916.2:n.348-29003_348-29000del
ENST00000404796.2:c.348-29003_348-29000del	ENSP00000385916.2:n.348-29003_348-29000del
NR_003529.3:n.371+5269_371+5272del
NR_047532.1:n.371+5269_371+5272del
NR_047533.1:n.371+5269_371+5272del
NR_047534.1:n.371+5269_371+5272del
NR_047535.1:n.371+5269_371+5272del
NR_047536.1:n.371+5269_371+5272del
NR_047537.1:n.371+5269_371+5272del
NR_047538.1:n.371+5269_371+5272del
NR_047539.1:n.371+5269_371+5272del
NR_047540.1:n.371+5269_371+5272del
NR_047541.1:n.371+5269_371+5272del
NR_047542.1:n.371+5269_371+5272del
NR_047543.1:n.371+5269_371+5272del
NR_120536.1:n.371+5269_371+5272del