Canonical Allele Identifier: CA383970548
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs1946497392

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718224C>G , CM000674.2:g.12718224C>G GRCh38
NC_000012.11:g.12871158C>G , CM000674.1:g.12871158C>G GRCh37
NC_000012.10:g.12762425C>G NCBI36
NG_016341.1:g.5857C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.385C>G ENSP00000507272.1:p.His129Asp
ENST00000682620.1:n.1631-601C>G
ENST00000684771.1:n.585-601C>G
ENST00000228872.9:c.385C>G MANE Select ENSP00000228872.4:p.His129Asp
ENST00000228872.8:c.385C>G ENSP00000228872.4:p.His129Asp
ENST00000396340.1:c.385C>G ENSP00000379629.1:p.His129Asp
ENST00000442489.1:c.193+171C>G ENSP00000407597.1:n.193+171C>G
ENST00000477087.1:n.155-601C>G
NM_004064.4:c.385C>G NP_004055.1:p.His129Asp
NM_004064.5:c.385C>G MANE Select NP_004055.1:p.His129Asp