Canonical Allele Identifier: CA2017047762
Gene: CDKN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718224C= , CM000674.2:g.12718224C= GRCh38
NC_000012.11:g.12871158C= , CM000674.1:g.12871158C= GRCh37
NC_000012.10:g.12762425C= NCBI36
NG_016341.1:g.5857C=

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.385C= ENSP00000507272.1:p.His129=
ENST00000682620.1:n.1631-601C=
ENST00000684771.1:n.585-601C=
ENST00000228872.9:c.385C= MANE Select ENSP00000228872.4:p.His129=
ENST00000228872.8:c.385C= ENSP00000228872.4:p.His129=
ENST00000396340.1:c.385C= ENSP00000379629.1:p.His129=
ENST00000442489.1:c.193+171C= ENSP00000407597.1:n.193+171C=
ENST00000477087.1:n.155-601C=
NM_004064.4:c.385C= NP_004055.1:p.His129=
NM_004064.5:c.385C= MANE Select NP_004055.1:p.His129=