Canonical Allele Identifier: CA944840035
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1710714
ClinVar RCV Id: RCV002292001
dbSNP Id: rs1946484698

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717823G>A , CM000674.2:g.12717823G>A GRCh38
NC_000012.11:g.12870757G>A , CM000674.1:g.12870757G>A GRCh37
NC_000012.10:g.12762024G>A NCBI36
NG_016341.1:g.5456G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.-17G>A ENSP00000507272.1:n.-17G>A
ENST00000682620.1:n.1631-1002G>A
ENST00000684771.1:n.585-1002G>A
ENST00000228872.9:c.-17G>A MANE Select ENSP00000228872.4:n.-17G>A
ENST00000228872.8:c.-17G>A ENSP00000228872.4:n.-17G>A
ENST00000396340.1:c.-17G>A ENSP00000379629.1:n.-17G>A
ENST00000477087.1:n.155-1002G>A
NM_004064.4:c.-17G>A NP_004055.1:n.-17G>A
NM_004064.5:c.-17G>A MANE Select NP_004055.1:n.-17G>A