Canonical Allele Identifier: CA191242141
Gene: CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs553493414
gnomAD v3: 9-22019577-G-A
gnomAD v4: 9-22019577-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22019577G>A , CM000671.2:g.22019577G>A GRCh38
NC_000009.11:g.22019576G>A , CM000671.1:g.22019576G>A GRCh37
NC_000009.10:g.22009576G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.348-9856G>A ENSP00000385916.2:n.348-9856G>A
ENST00000404796.2:c.348-9856G>A ENSP00000385916.2:n.348-9856G>A
NR_003529.3:n.372-9856G>A
NR_047532.1:n.372-9856G>A
NR_047533.1:n.371+24416G>A
NR_047534.1:n.371+24416G>A
NR_047535.1:n.371+24416G>A
NR_047536.1:n.371+24416G>A
NR_047537.1:n.371+24416G>A
NR_047538.1:n.371+24416G>A
NR_047539.1:n.372-9856G>A
NR_047540.1:n.371+24416G>A
NR_047541.1:n.371+24416G>A
NR_047542.1:n.371+24416G>A
NR_047543.1:n.371+24416G>A
NR_120536.1:n.371+24416G>A