Canonical Allele Identifier: CA383970558
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs377573215

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718226T>A , CM000674.2:g.12718226T>A GRCh38
NC_000012.11:g.12871160T>A , CM000674.1:g.12871160T>A GRCh37
NC_000012.10:g.12762427T>A NCBI36
NG_016341.1:g.5859T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.387T>A ENSP00000507272.1:p.His129Gln
ENST00000682620.1:n.1631-599T>A
ENST00000684771.1:n.585-599T>A
ENST00000228872.9:c.387T>A MANE Select ENSP00000228872.4:p.His129Gln
ENST00000228872.8:c.387T>A ENSP00000228872.4:p.His129Gln
ENST00000396340.1:c.387T>A ENSP00000379629.1:p.His129Gln
ENST00000442489.1:c.193+173T>A ENSP00000407597.1:n.193+173T>A
ENST00000477087.1:n.155-599T>A
NM_004064.4:c.387T>A NP_004055.1:p.His129Gln
NM_004064.5:c.387T>A MANE Select NP_004055.1:p.His129Gln