Canonical Allele Identifier: CA2017047628
Gene: CDKN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718050G= , CM000674.2:g.12718050G= GRCh38
NC_000012.11:g.12870984G= , CM000674.1:g.12870984G= GRCh37
NC_000012.10:g.12762251G= NCBI36
NG_016341.1:g.5683G=

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.211G= ENSP00000507272.1:p.Glu71=
ENST00000682620.1:n.1631-775G=
ENST00000684771.1:n.585-775G=
ENST00000228872.9:c.211G= MANE Select ENSP00000228872.4:p.Glu71=
ENST00000228872.8:c.211G= ENSP00000228872.4:p.Glu71=
ENST00000396340.1:c.211G= ENSP00000379629.1:p.Glu71=
ENST00000442489.1:c.190G= ENSP00000407597.1:p.Glu64=
ENST00000477087.1:n.155-775G=
NM_004064.4:c.211G= NP_004055.1:p.Glu71=
NM_004064.5:c.211G= MANE Select NP_004055.1:p.Glu71=