Canonical Allele Identifier: CA6457461
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 259226
dbSNP Id: rs2066827

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718165T>G , CM000674.2:g.12718165T>G GRCh38
NC_000012.11:g.12871099T>G , CM000674.1:g.12871099T>G GRCh37
NC_000012.10:g.12762366T>G NCBI36
NG_016341.1:g.5798T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.326T>G ENSP00000507272.1:p.Val109Gly
ENST00000682620.1:n.1631-660T>G
ENST00000684771.1:n.585-660T>G
ENST00000228872.9:c.326T>G MANE Select ENSP00000228872.4:p.Val109Gly
ENST00000228872.8:c.326T>G ENSP00000228872.4:p.Val109Gly
ENST00000396340.1:c.326T>G ENSP00000379629.1:p.Val109Gly
ENST00000442489.1:c.193+112T>G ENSP00000407597.1:n.193+112T>G
ENST00000477087.1:n.155-660T>G
NM_004064.4:c.326T>G NP_004055.1:p.Val109Gly
NM_004064.5:c.326T>G MANE Select NP_004055.1:p.Val109Gly