Canonical Allele Identifier: CA383970645
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs546234840

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718246A>C , CM000674.2:g.12718246A>C GRCh38
NC_000012.11:g.12871180A>C , CM000674.1:g.12871180A>C GRCh37
NC_000012.10:g.12762447A>C NCBI36
NG_016341.1:g.5879A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.407A>C ENSP00000507272.1:p.Asp136Ala
ENST00000682620.1:n.1631-579A>C
ENST00000684771.1:n.585-579A>C
ENST00000228872.9:c.407A>C MANE Select ENSP00000228872.4:p.Asp136Ala
ENST00000228872.8:c.407A>C ENSP00000228872.4:p.Asp136Ala
ENST00000396340.1:c.407A>C ENSP00000379629.1:p.Asp136Ala
ENST00000442489.1:c.193+193A>C ENSP00000407597.1:n.193+193A>C
ENST00000477087.1:n.155-579A>C
NM_004064.4:c.407A>C NP_004055.1:p.Asp136Ala
NM_004064.5:c.407A>C MANE Select NP_004055.1:p.Asp136Ala