Canonical Allele Identifier: CA862190662
Gene: CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1402616220
MyVariant Identifiers: chr9:g.22000136del (hg19) chr9:g.22000137del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22000138del , CM000671.2:g.22000138del GRCh38
NC_000009.11:g.22000137del , CM000671.1:g.22000137del GRCh37
NC_000009.10:g.21990137del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.348-29295del ENSP00000385916.2:n.348-29295del
ENST00000404796.2:c.348-29295del ENSP00000385916.2:n.348-29295del
NR_003529.3:n.371+4977del
NR_047532.1:n.371+4977del
NR_047533.1:n.371+4977del
NR_047534.1:n.371+4977del
NR_047535.1:n.371+4977del
NR_047536.1:n.371+4977del
NR_047537.1:n.371+4977del
NR_047538.1:n.371+4977del
NR_047539.1:n.371+4977del
NR_047540.1:n.371+4977del
NR_047541.1:n.371+4977del
NR_047542.1:n.371+4977del
NR_047543.1:n.371+4977del
NR_120536.1:n.371+4977del
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