Canonical Allele Identifier: CA383970300
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs755989911

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718180C>A , CM000674.2:g.12718180C>A GRCh38
NC_000012.11:g.12871114C>A , CM000674.1:g.12871114C>A GRCh37
NC_000012.10:g.12762381C>A NCBI36
NG_016341.1:g.5813C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.341C>A ENSP00000507272.1:p.Pro114Gln
ENST00000682620.1:n.1631-645C>A
ENST00000684771.1:n.585-645C>A
ENST00000228872.9:c.341C>A MANE Select ENSP00000228872.4:p.Pro114Gln
ENST00000228872.8:c.341C>A ENSP00000228872.4:p.Pro114Gln
ENST00000396340.1:c.341C>A ENSP00000379629.1:p.Pro114Gln
ENST00000442489.1:c.193+127C>A ENSP00000407597.1:n.193+127C>A
ENST00000477087.1:n.155-645C>A
NM_004064.4:c.341C>A NP_004055.1:p.Pro114Gln
NM_004064.5:c.341C>A MANE Select NP_004055.1:p.Pro114Gln