Canonical Allele Identifier: CA2573147859
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1425912
ClinVar RCV Id: RCV001927000
dbSNP Id: rs2136355726

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718020_12718157del , CM000674.2:g.12718020_12718157del GRCh38
NC_000012.11:g.12870954_12871091del , CM000674.1:g.12870954_12871091del GRCh37
NC_000012.10:g.12762221_12762358del NCBI36
NG_016341.1:g.5653_5790del

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.181_318del ENSP00000507272.1:p.Asn61_Ser106del
ENST00000682620.1:n.1631-805_1631-668del
ENST00000684771.1:n.585-805_585-668del
ENST00000228872.9:c.181_318del MANE Select ENSP00000228872.4:p.Asn61_Ser106del
ENST00000228872.8:c.181_318del ENSP00000228872.4:p.Asn61_Ser106del
ENST00000396340.1:c.181_318del ENSP00000379629.1:p.Asn61_Ser106del
ENST00000442489.1:c.160_193+104del
ENST00000477087.1:n.155-805_155-668del
NM_004064.4:c.181_318del NP_004055.1:p.Asn61_Ser106del
NM_004064.5:c.181_318del MANE Select NP_004055.1:p.Asn61_Ser106del