Canonical Allele Identifier: CA383970734
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 852895
ClinVar RCV Id: RCV001057606
dbSNP Id: rs1946499047

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718266G>A , CM000674.2:g.12718266G>A GRCh38
NC_000012.11:g.12871200G>A , CM000674.1:g.12871200G>A GRCh37
NC_000012.10:g.12762467G>A NCBI36
NG_016341.1:g.5899G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.427G>A ENSP00000507272.1:p.Gly143Arg
ENST00000682620.1:n.1631-559G>A
ENST00000684771.1:n.585-559G>A
ENST00000228872.9:c.427G>A MANE Select ENSP00000228872.4:p.Gly143Arg
ENST00000228872.8:c.427G>A ENSP00000228872.4:p.Gly143Arg
ENST00000396340.1:c.427G>A ENSP00000379629.1:p.Gly143Arg
ENST00000442489.1:c.193+213G>A ENSP00000407597.1:n.193+213G>A
ENST00000477087.1:n.155-559G>A
NM_004064.4:c.427G>A NP_004055.1:p.Gly143Arg
NM_004064.5:c.427G>A MANE Select NP_004055.1:p.Gly143Arg