Canonical Allele Identifier: CA5012662
Gene: CDKN2B-AS1 HGNC NCBI
COSMIC:
COSN8811054
COSN15315634 (not active)
MyVariant.info:
GRCh38 chr9:g.22029548T>C
GRCh37 chr9:g.22029547T>C
gnomAD v2:
9:22029547 T / C
gnomAD v3:
9:22029548 T / C
gnomAD v4:
chr9-22029548-T-C
Joint Max Group AF 0.41175042 (NFE)
Genomes Max Group AF 0.41034042 (NFE)
Exomes Max Group AF 0.41140255 (NFE)
dbSNP:
564398
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22029548T>C , CM000671.2:g.22029548T>C GRCh38
NC_000009.11:g.22029547T>C , CM000671.1:g.22029547T>C GRCh37
NC_000009.10:g.22019547T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.*31T>C ENSP00000385916.2:n.*31T>C
ENST00000404796.2:c.*31T>C ENSP00000385916.2:n.*31T>C
NR_003529.3:n.487T>C
NR_047532.1:n.487T>C
NR_047533.1:n.372-17203T>C
NR_047534.1:n.372-17203T>C
NR_047535.1:n.372-17203T>C
NR_047536.1:n.372-17203T>C
NR_047537.1:n.372-17203T>C
NR_047538.1:n.372-17203T>C
NR_047539.1:n.487T>C
NR_047540.1:n.372-17203T>C
NR_047541.1:n.372-17203T>C
NR_047542.1:n.372-17203T>C
NR_047543.1:n.372-17203T>C
NR_120536.1:n.372-17203T>C
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