Canonical Allele Identifier: CA13614122
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs34329

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12720299G>C , CM000674.2:g.12720299G>C GRCh38
NC_000012.11:g.12873233G>C , CM000674.1:g.12873233G>C GRCh37
NC_000012.10:g.12764500G>C NCBI36
NG_016341.1:g.7932G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000228872.9:c.*9-737G>C MANE Select ENSP00000228872.4:p.=
ENST00000228872.8:c.*9-737G>C ENSP00000228872.4:p.=
ENST00000396340.1:c.476-766G>C ENSP00000379629.1:p.=
ENST00000442489.1:n.324-737G>C ENSP00000407597.1:p.=
ENST00000477087.1:n.285-737G>C
NM_004064.4:c.*9-737G>C NP_004055.1:p.=
NM_004064.5:c.*9-737G>C MANE Select NP_004055.1:p.=