Canonical Allele Identifier: CA1122168569
Gene: CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1820870059
gnomAD v3: 9-22000440-G-A
gnomAD v4: 9-22000440-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22000440G>A , CM000671.2:g.22000440G>A GRCh38
NC_000009.11:g.22000439G>A , CM000671.1:g.22000439G>A GRCh37
NC_000009.10:g.21990439G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.348-28993G>A ENSP00000385916.2:n.348-28993G>A
ENST00000404796.2:c.348-28993G>A ENSP00000385916.2:n.348-28993G>A
NR_003529.3:n.371+5279G>A
NR_047532.1:n.371+5279G>A
NR_047533.1:n.371+5279G>A
NR_047534.1:n.371+5279G>A
NR_047535.1:n.371+5279G>A
NR_047536.1:n.371+5279G>A
NR_047537.1:n.371+5279G>A
NR_047538.1:n.371+5279G>A
NR_047539.1:n.371+5279G>A
NR_047540.1:n.371+5279G>A
NR_047541.1:n.371+5279G>A
NR_047542.1:n.371+5279G>A
NR_047543.1:n.371+5279G>A
NR_120536.1:n.371+5279G>A
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