Canonical Allele Identifier: CA684983022
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs1467096405

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12720271G>A , CM000674.2:g.12720271G>A GRCh38
NC_000012.11:g.12873205G>A , CM000674.1:g.12873205G>A GRCh37
NC_000012.10:g.12764472G>A NCBI36
NG_016341.1:g.7904G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.*1325G>A ENSP00000507272.1:n.*1325G>A
ENST00000682620.1:n.1761-765G>A
ENST00000684771.1:n.715-765G>A
ENST00000228872.9:c.*9-765G>A MANE Select ENSP00000228872.4:n.*9-765G>A
ENST00000228872.8:c.*9-765G>A ENSP00000228872.4:n.*9-765G>A
ENST00000396340.1:c.476-794G>A ENSP00000379629.1:n.476-794G>A
ENST00000442489.1:c.324-765G>A ENSP00000407597.1:n.324-765G>A
ENST00000477087.1:n.285-765G>A
NM_004064.4:c.*9-765G>A NP_004055.1:n.*9-765G>A
NM_004064.5:c.*9-765G>A MANE Select NP_004055.1:n.*9-765G>A