Canonical Allele Identifier: CA186089
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs774454456

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717811_12717814del , CM000674.2:g.12717811_12717814del GRCh38
NC_000012.11:g.12870745_12870748del , CM000674.1:g.12870745_12870748del GRCh37
NC_000012.10:g.12762012_12762015del NCBI36
NG_016341.1:g.5444_5447del

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.-29_-26del ENSP00000507272.1:n.-29_-26del
ENST00000682620.1:n.1631-1014_1631-1011del
ENST00000684771.1:n.585-1014_585-1011del
ENST00000228872.9:c.-29_-26del MANE Select ENSP00000228872.4:n.-29_-26del
ENST00000228872.8:c.-29_-26del ENSP00000228872.4:n.-29_-26del
ENST00000477087.1:n.155-1014_155-1011del
NM_004064.4:c.-29_-26del NP_004055.1:n.-29_-26del
NM_004064.5:c.-29_-26del MANE Select NP_004055.1:n.-29_-26del