Canonical Allele Identifier: CA586900081
Gene: CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1473487862
gnomAD v2: 9-22010048-CTTTG-C
gnomAD v3: 9-22010049-CTTTG-C
gnomAD v4: 9-22010049-CTTTG-C
MyVariant Identifiers: chr9:g.22010049_22010052del (hg19) chr9:g.22010050_22010053del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22010054_22010057del , CM000671.2:g.22010054_22010057del GRCh38
NC_000009.11:g.22010053_22010056del , CM000671.1:g.22010053_22010056del GRCh37
NC_000009.10:g.22000053_22000056del NCBI36
NG_023297.1:g.4261_4264del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.348-19379_348-19376del ENSP00000385916.2:n.348-19379_348-19376del
ENST00000404796.2:c.348-19379_348-19376del ENSP00000385916.2:n.348-19379_348-19376del
NR_003529.3:n.371+14893_371+14896del
NR_047532.1:n.371+14893_371+14896del
NR_047533.1:n.371+14893_371+14896del
NR_047534.1:n.371+14893_371+14896del
NR_047535.1:n.371+14893_371+14896del
NR_047536.1:n.371+14893_371+14896del
NR_047537.1:n.371+14893_371+14896del
NR_047538.1:n.371+14893_371+14896del
NR_047539.1:n.371+14893_371+14896del
NR_047540.1:n.371+14893_371+14896del
NR_047541.1:n.371+14893_371+14896del
NR_047542.1:n.371+14893_371+14896del
NR_047543.1:n.371+14893_371+14896del
NR_120536.1:n.371+14893_371+14896del
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