Canonical Allele Identifier: CA12951952
Gene: CDKN2B-AS1 HGNC NCBI
COSMIC:
COSN14871187 (not active)
MyVariant.info:
GRCh38 chr9:g.22031006G>A
GRCh37 chr9:g.22031005G>A
gnomAD v2:
9:22031005 G / A
gnomAD v3:
9:22031006 G / A
gnomAD v4:
chr9-22031006-G-A
Joint Max Group AF 0.91802157 (AFR)
Genomes Max Group AF 0.91802157 (AFR)
dbSNP:
7865618
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22031006G>A , CM000671.2:g.22031006G>A GRCh38
NC_000009.11:g.22031005G>A , CM000671.1:g.22031005G>A GRCh37
NC_000009.10:g.22021005G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.2:c.*77+1412G>A ENSP00000385916.2:n.*77+1412G>A
NR_003529.3:n.533+1412G>A
NR_047532.1:n.533+1412G>A
NR_047533.1:n.372-15745G>A
NR_047534.1:n.372-15745G>A
NR_047535.1:n.372-15745G>A
NR_047536.1:n.372-15745G>A
NR_047537.1:n.372-15745G>A
NR_047538.1:n.372-15745G>A
NR_047539.1:n.533+1412G>A
NR_047540.1:n.372-15745G>A
NR_047541.1:n.372-15745G>A
NR_047542.1:n.372-15745G>A
NR_047543.1:n.372-15745G>A
NR_120536.1:n.372-15745G>A
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