Canonical Allele Identifier: CA478845497
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2002429
ClinVar RCV Id: RCV002832969
dbSNP Id: rs146161282
MyVariant Identifiers: chr12:g.12871049G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718115G>C , CM000674.2:g.12718115G>C GRCh38
NC_000012.11:g.12871049G>C , CM000674.1:g.12871049G>C GRCh37
NC_000012.10:g.12762316G>C NCBI36
NG_016341.1:g.5748G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.276G>C ENSP00000507272.1:p.Pro92=
ENST00000682620.1:n.1631-710G>C
ENST00000684771.1:n.585-710G>C
ENST00000228872.9:c.276G>C MANE Select ENSP00000228872.4:p.Pro92=
ENST00000228872.8:c.276G>C ENSP00000228872.4:p.Pro92=
ENST00000396340.1:c.276G>C ENSP00000379629.1:p.Pro92=
ENST00000442489.1:c.193+62G>C ENSP00000407597.1:n.193+62G>C
ENST00000477087.1:n.155-710G>C
NM_004064.4:c.276G>C NP_004055.1:p.Pro92=
NM_004064.5:c.276G>C MANE Select NP_004055.1:p.Pro92=