Canonical Allele Identifier: CA862190828
Gene: CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1464386203
gnomAD v3: 9-22000496-A-G
gnomAD v4: 9-22000496-A-G
MyVariant Identifiers: chr9:g.22000495A>G (hg19) chr9:g.22000496A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22000496A>G , CM000671.2:g.22000496A>G GRCh38
NC_000009.11:g.22000495A>G , CM000671.1:g.22000495A>G GRCh37
NC_000009.10:g.21990495A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.348-28937A>G ENSP00000385916.2:n.348-28937A>G
ENST00000404796.2:c.348-28937A>G ENSP00000385916.2:n.348-28937A>G
NR_003529.3:n.371+5335A>G
NR_047532.1:n.371+5335A>G
NR_047533.1:n.371+5335A>G
NR_047534.1:n.371+5335A>G
NR_047535.1:n.371+5335A>G
NR_047536.1:n.371+5335A>G
NR_047537.1:n.371+5335A>G
NR_047538.1:n.371+5335A>G
NR_047539.1:n.371+5335A>G
NR_047540.1:n.371+5335A>G
NR_047541.1:n.371+5335A>G
NR_047542.1:n.371+5335A>G
NR_047543.1:n.371+5335A>G
NR_120536.1:n.371+5335A>G
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