Canonical Allele Identifier: CA587082047
Gene: CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1301809250
gnomAD v2: 9-22019587-G-C
gnomAD v3: 9-22019588-G-C
gnomAD v4: 9-22019588-G-C
MyVariant Identifiers: chr9:g.22019587G>C (hg19) chr9:g.22019588G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22019588G>C , CM000671.2:g.22019588G>C GRCh38
NC_000009.11:g.22019587G>C , CM000671.1:g.22019587G>C GRCh37
NC_000009.10:g.22009587G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.348-9845G>C ENSP00000385916.2:n.348-9845G>C
ENST00000404796.2:c.348-9845G>C ENSP00000385916.2:n.348-9845G>C
NR_003529.3:n.372-9845G>C
NR_047532.1:n.372-9845G>C
NR_047533.1:n.371+24427G>C
NR_047534.1:n.371+24427G>C
NR_047535.1:n.371+24427G>C
NR_047536.1:n.371+24427G>C
NR_047537.1:n.371+24427G>C
NR_047538.1:n.371+24427G>C
NR_047539.1:n.372-9845G>C
NR_047540.1:n.371+24427G>C
NR_047541.1:n.371+24427G>C
NR_047542.1:n.371+24427G>C
NR_047543.1:n.371+24427G>C
NR_120536.1:n.371+24427G>C
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