Canonical Allele Identifier: CA383969134
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs1465844938

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718005A>G , CM000674.2:g.12718005A>G GRCh38
NC_000012.11:g.12870939A>G , CM000674.1:g.12870939A>G GRCh37
NC_000012.10:g.12762206A>G NCBI36
NG_016341.1:g.5638A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.166A>G ENSP00000507272.1:p.Ser56Gly
ENST00000682620.1:n.1631-820A>G
ENST00000684771.1:n.585-820A>G
ENST00000228872.9:c.166A>G MANE Select ENSP00000228872.4:p.Ser56Gly
ENST00000228872.8:c.166A>G ENSP00000228872.4:p.Ser56Gly
ENST00000396340.1:c.166A>G ENSP00000379629.1:p.Ser56Gly
ENST00000442489.1:c.145A>G ENSP00000407597.1:p.Ser49Gly
ENST00000477087.1:n.155-820A>G
NM_004064.4:c.166A>G NP_004055.1:p.Ser56Gly
NM_004064.5:c.166A>G MANE Select NP_004055.1:p.Ser56Gly