Canonical Allele Identifier: CA191248721
Gene: CDKN2B-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.22072302G>C
GRCh37 chr9:g.22072301G>C
gnomAD v2:
9:22072301 G / C
gnomAD v3:
9:22072302 G / C
gnomAD v4:
chr9-22072302-G-C
Joint Max Group AF 0.89810485 (AFR)
Genomes Max Group AF 0.89810485 (AFR)
ClinVar RCV:
RCV001003463
ClinVar Variation:
812645
dbSNP:
9632884
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22072302G>C , CM000671.2:g.22072302G>C GRCh38
NC_000009.11:g.22072301G>C , CM000671.1:g.22072301G>C GRCh37
NC_000009.10:g.22062301G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003529.3:n.2448+5949G>C
NR_047532.1:n.1075+15915G>C
NR_047533.1:n.645-5377G>C
NR_047534.1:n.644+23074G>C
NR_047535.1:n.780+15915G>C
NR_047536.1:n.644+23074G>C
NR_047537.1:n.780+15915G>C
NR_047538.1:n.644+23074G>C
NR_047539.1:n.2449-5377G>C
NR_047540.1:n.1049-5377G>C
NR_047541.1:n.856-5377G>C
NR_047542.1:n.781-5377G>C
NR_047543.1:n.780+15915G>C
NR_120536.1:n.644+23074G>C
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