Canonical Allele Identifier: CA6457382
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1691538
ClinVar RCV Id: RCV002254867 RCV002337416
dbSNP Id: rs765527234
ExAC: 12:12870891 G / A
gnomAD v2: 12-12870891-G-A
gnomAD v4: 12-12717957-G-A
COSMIC: COSM4384673
MyVariant Identifiers: chr12:g.12870891G>A (hg19) chr12:g.12717957G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717957G>A , CM000674.2:g.12717957G>A GRCh38
NC_000012.11:g.12870891G>A , CM000674.1:g.12870891G>A GRCh37
NC_000012.10:g.12762158G>A NCBI36
NG_016341.1:g.5590G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.118G>A ENSP00000507272.1:p.Glu40Lys
ENST00000682620.1:n.1631-868G>A
ENST00000684771.1:n.585-868G>A
ENST00000228872.9:c.118G>A MANE Select ENSP00000228872.4:p.Glu40Lys
ENST00000228872.8:c.118G>A ENSP00000228872.4:p.Glu40Lys
ENST00000396340.1:c.118G>A ENSP00000379629.1:p.Glu40Lys
ENST00000442489.1:c.97G>A ENSP00000407597.1:p.Glu33Lys
ENST00000477087.1:n.155-868G>A
NM_004064.4:c.118G>A NP_004055.1:p.Glu40Lys
NM_004064.5:c.118G>A MANE Select NP_004055.1:p.Glu40Lys
Search 100 bp 5'
Search 100 bp 3'