Canonical Allele Identifier: CA603494652
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs1245541652

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717827A>G , CM000674.2:g.12717827A>G GRCh38
NC_000012.11:g.12870761A>G , CM000674.1:g.12870761A>G GRCh37
NC_000012.10:g.12762028A>G NCBI36
NG_016341.1:g.5460A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.-13A>G ENSP00000507272.1:n.-13A>G
ENST00000682620.1:n.1631-998A>G
ENST00000684771.1:n.585-998A>G
ENST00000228872.9:c.-13A>G MANE Select ENSP00000228872.4:n.-13A>G
ENST00000228872.8:c.-13A>G ENSP00000228872.4:n.-13A>G
ENST00000396340.1:c.-13A>G ENSP00000379629.1:n.-13A>G
ENST00000477087.1:n.155-998A>G
NM_004064.4:c.-13A>G NP_004055.1:n.-13A>G
NM_004064.5:c.-13A>G MANE Select NP_004055.1:n.-13A>G