Canonical Allele Identifier: CA383970540
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs761235464

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718222C>A , CM000674.2:g.12718222C>A GRCh38
NC_000012.11:g.12871156C>A , CM000674.1:g.12871156C>A GRCh37
NC_000012.10:g.12762423C>A NCBI36
NG_016341.1:g.5855C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.383C>A ENSP00000507272.1:p.Thr128Lys
ENST00000682620.1:n.1631-603C>A
ENST00000684771.1:n.585-603C>A
ENST00000228872.9:c.383C>A MANE Select ENSP00000228872.4:p.Thr128Lys
ENST00000228872.8:c.383C>A ENSP00000228872.4:p.Thr128Lys
ENST00000396340.1:c.383C>A ENSP00000379629.1:p.Thr128Lys
ENST00000442489.1:c.193+169C>A ENSP00000407597.1:n.193+169C>A
ENST00000477087.1:n.155-603C>A
NM_004064.4:c.383C>A NP_004055.1:p.Thr128Lys
NM_004064.5:c.383C>A MANE Select NP_004055.1:p.Thr128Lys