Canonical Allele Identifier: CA13008916
Gene: CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs495490
gnomAD v2: 9-22010412-A-G
gnomAD v3: 9-22010413-A-G
gnomAD v4: 9-22010413-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22010413A>G , CM000671.2:g.22010413A>G GRCh38
NC_000009.11:g.22010412A>G , CM000671.1:g.22010412A>G GRCh37
NC_000009.10:g.22000412A>G NCBI36
NG_023297.1:g.3901T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000404796.3:c.348-19020A>G ENSP00000385916.2:n.348-19020A>G
ENST00000404796.2:c.348-19020A>G ENSP00000385916.2:n.348-19020A>G
NR_003529.3:n.371+15252A>G
NR_047532.1:n.371+15252A>G
NR_047533.1:n.371+15252A>G
NR_047534.1:n.371+15252A>G
NR_047535.1:n.371+15252A>G
NR_047536.1:n.371+15252A>G
NR_047537.1:n.371+15252A>G
NR_047538.1:n.371+15252A>G
NR_047539.1:n.371+15252A>G
NR_047540.1:n.371+15252A>G
NR_047541.1:n.371+15252A>G
NR_047542.1:n.371+15252A>G
NR_047543.1:n.371+15252A>G
NR_120536.1:n.371+15252A>G