Canonical Allele Identifier: CA2017048991
Gene: CDKN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12720397G= , CM000674.2:g.12720397G= GRCh38
NC_000012.11:g.12873331G= , CM000674.1:g.12873331G= GRCh37
NC_000012.10:g.12764598G= NCBI36
NG_016341.1:g.8030G=

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.*1451G= ENSP00000507272.1:n.*1451G=
ENST00000682620.1:n.1761-639G=
ENST00000684771.1:n.715-639G=
ENST00000228872.9:c.*9-639G= MANE Select ENSP00000228872.4:n.*9-639G=
ENST00000228872.8:c.*9-639G= ENSP00000228872.4:n.*9-639G=
ENST00000396340.1:c.476-668G= ENSP00000379629.1:n.476-668G=
ENST00000442489.1:c.324-639G= ENSP00000407597.1:n.324-639G=
ENST00000477087.1:n.285-639G=
NM_004064.4:c.*9-639G= NP_004055.1:n.*9-639G=
NM_004064.5:c.*9-639G= MANE Select NP_004055.1:n.*9-639G=