Canonical Allele Identifier: CA383969193
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1481324
ClinVar RCV Id: RCV001994152 RCV002407236
dbSNP Id: rs1349254230
gnomAD v4: 12-12718011-C-T
MyVariant Identifiers: chr12:g.12870945C>T (hg19) chr12:g.12718011C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718011C>T , CM000674.2:g.12718011C>T GRCh38
NC_000012.11:g.12870945C>T , CM000674.1:g.12870945C>T GRCh37
NC_000012.10:g.12762212C>T NCBI36
NG_016341.1:g.5644C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.172C>T ENSP00000507272.1:p.Arg58Cys
ENST00000682620.1:n.1631-814C>T
ENST00000684771.1:n.585-814C>T
ENST00000228872.9:c.172C>T MANE Select ENSP00000228872.4:p.Arg58Cys
ENST00000228872.8:c.172C>T ENSP00000228872.4:p.Arg58Cys
ENST00000396340.1:c.172C>T ENSP00000379629.1:p.Arg58Cys
ENST00000442489.1:c.151C>T ENSP00000407597.1:p.Arg51Cys
ENST00000477087.1:n.155-814C>T
NM_004064.4:c.172C>T NP_004055.1:p.Arg58Cys
NM_004064.5:c.172C>T MANE Select NP_004055.1:p.Arg58Cys
Search 100 bp 5'
Search 100 bp 3'