Canonical Allele Identifier: CA478845439
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1767884
dbSNP Id: rs1202654522

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717935C>T , CM000674.2:g.12717935C>T GRCh38
NC_000012.11:g.12870869C>T , CM000674.1:g.12870869C>T GRCh37
NC_000012.10:g.12762136C>T NCBI36
NG_016341.1:g.5568C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.96C>T ENSP00000507272.1:p.Leu32=
ENST00000682620.1:n.1631-890C>T
ENST00000684771.1:n.585-890C>T
ENST00000228872.9:c.96C>T MANE Select ENSP00000228872.4:p.Leu32=
ENST00000228872.8:c.96C>T ENSP00000228872.4:p.Leu32=
ENST00000396340.1:c.96C>T ENSP00000379629.1:p.Leu32=
ENST00000442489.1:c.75C>T ENSP00000407597.1:p.Leu25=
ENST00000477087.1:n.155-890C>T
NM_004064.4:c.96C>T NP_004055.1:p.Leu32=
NM_004064.5:c.96C>T MANE Select NP_004055.1:p.Leu32=