Canonical Allele Identifier: CA2739271873

Gene: CDKN1B

Linked Data

• ClinVar Variation Id: 2809877
• ClinVar RCV Id: RCV003620694

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718326T>C , CM000674.2:g.12718326T>C	GRCh38
NC_000012.11:g.12871260T>C , CM000674.1:g.12871260T>C	GRCh37
NC_000012.10:g.12762527T>C	NCBI36
NG_016341.1:g.5959T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.475+12T>C	ENSP00000507272.1:n.475+12T>C
ENST00000682620.1:n.1631-499T>C
ENST00000684771.1:n.585-499T>C
ENST00000228872.9:c.475+12T>C MANE Select	ENSP00000228872.4:n.475+12T>C
ENST00000228872.8:c.475+12T>C	ENSP00000228872.4:n.475+12T>C
ENST00000396340.1:c.475+12T>C	ENSP00000379629.1:n.475+12T>C
ENST00000442489.1:c.193+273T>C	ENSP00000407597.1:n.193+273T>C
ENST00000477087.1:n.155-499T>C
NM_004064.4:c.475+12T>C	NP_004055.1:n.475+12T>C
NM_004064.5:c.475+12T>C MANE Select	NP_004055.1:n.475+12T>C