Canonical Allele Identifier: CA2017047632
Gene: CDKN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718053G= , CM000674.2:g.12718053G= GRCh38
NC_000012.11:g.12870987G= , CM000674.1:g.12870987G= GRCh37
NC_000012.10:g.12762254G= NCBI36
NG_016341.1:g.5686G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.214G= ENSP00000507272.1:p.Gly72=
ENST00000682620.1:n.1631-772G=
ENST00000684771.1:n.585-772G=
ENST00000228872.9:c.214G= MANE Select ENSP00000228872.4:p.Gly72=
ENST00000228872.8:c.214G= ENSP00000228872.4:p.Gly72=
ENST00000396340.1:c.214G= ENSP00000379629.1:p.Gly72=
ENST00000442489.1:c.193G= ENSP00000407597.1:p.Asp65=
ENST00000477087.1:n.155-772G=
NM_004064.4:c.214G= NP_004055.1:p.Gly72=
NM_004064.5:c.214G= MANE Select NP_004055.1:p.Gly72=