Canonical Allele Identifier: CA6457401
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 948905
ClinVar RCV Id: RCV001220252 RCV002402662 RCV003238846
dbSNP Id: rs758686055
ExAC: 12:12870940 G / C
gnomAD v2: 12-12870940-G-C
gnomAD v4: 12-12718006-G-C
MyVariant Identifiers: chr12:g.12870940G>C (hg19) chr12:g.12718006G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718006G>C , CM000674.2:g.12718006G>C GRCh38
NC_000012.11:g.12870940G>C , CM000674.1:g.12870940G>C GRCh37
NC_000012.10:g.12762207G>C NCBI36
NG_016341.1:g.5639G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.167G>C ENSP00000507272.1:p.Ser56Thr
ENST00000682620.1:n.1631-819G>C
ENST00000684771.1:n.585-819G>C
ENST00000228872.9:c.167G>C MANE Select ENSP00000228872.4:p.Ser56Thr
ENST00000228872.8:c.167G>C ENSP00000228872.4:p.Ser56Thr
ENST00000396340.1:c.167G>C ENSP00000379629.1:p.Ser56Thr
ENST00000442489.1:c.146G>C ENSP00000407597.1:p.Ser49Thr
ENST00000477087.1:n.155-819G>C
NM_004064.4:c.167G>C NP_004055.1:p.Ser56Thr
NM_004064.5:c.167G>C MANE Select NP_004055.1:p.Ser56Thr
Search 100 bp 5'
Search 100 bp 3'