Canonical Allele Identifier: CA383968055
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1014136
ClinVar RCV Id: RCV001312831
dbSNP Id: rs775772074
MyVariant Identifiers: chr12:g.12870808G>C (hg19) chr12:g.12717874G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717874G>C , CM000674.2:g.12717874G>C GRCh38
NC_000012.11:g.12870808G>C , CM000674.1:g.12870808G>C GRCh37
NC_000012.10:g.12762075G>C NCBI36
NG_016341.1:g.5507G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.35G>C ENSP00000507272.1:p.Ser12Thr
ENST00000682620.1:n.1631-951G>C
ENST00000684771.1:n.585-951G>C
ENST00000228872.9:c.35G>C MANE Select ENSP00000228872.4:p.Ser12Thr
ENST00000228872.8:c.35G>C ENSP00000228872.4:p.Ser12Thr
ENST00000396340.1:c.35G>C ENSP00000379629.1:p.Ser12Thr
ENST00000442489.1:c.14G>C ENSP00000407597.1:p.Ser5Thr
ENST00000477087.1:n.155-951G>C
NM_004064.4:c.35G>C NP_004055.1:p.Ser12Thr
NM_004064.5:c.35G>C MANE Select NP_004055.1:p.Ser12Thr
Search 100 bp 5'
Search 100 bp 3'