Canonical Allele Identifier: CA233062725
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs917794000
MyVariant Identifiers: chr12:g.12720081A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12720081A>T , CM000674.2:g.12720081A>T GRCh38
NC_000012.11:g.12873015A>T , CM000674.1:g.12873015A>T GRCh37
NC_000012.10:g.12764282A>T NCBI36
NG_016341.1:g.7714A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.*1135A>T ENSP00000507272.1:n.*1135A>T
ENST00000682620.1:n.1761-955A>T
ENST00000684771.1:n.715-955A>T
ENST00000228872.9:c.*9-955A>T MANE Select ENSP00000228872.4:n.*9-955A>T
ENST00000228872.8:c.*9-955A>T ENSP00000228872.4:n.*9-955A>T
ENST00000396340.1:c.476-984A>T ENSP00000379629.1:n.476-984A>T
ENST00000442489.1:c.324-955A>T ENSP00000407597.1:n.324-955A>T
ENST00000477087.1:n.285-955A>T
NM_004064.4:c.*9-955A>T NP_004055.1:n.*9-955A>T
NM_004064.5:c.*9-955A>T MANE Select NP_004055.1:n.*9-955A>T