Canonical Allele Identifier: CA478845339
Gene: CDKN1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.12870816C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717882C>A , CM000674.2:g.12717882C>A GRCh38
NC_000012.11:g.12870816C>A , CM000674.1:g.12870816C>A GRCh37
NC_000012.10:g.12762083C>A NCBI36
NG_016341.1:g.5515C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.43C>A ENSP00000507272.1:p.Arg15=
ENST00000682620.1:n.1631-943C>A
ENST00000684771.1:n.585-943C>A
ENST00000228872.9:c.43C>A MANE Select ENSP00000228872.4:p.Arg15=
ENST00000228872.8:c.43C>A ENSP00000228872.4:p.Arg15=
ENST00000396340.1:c.43C>A ENSP00000379629.1:p.Arg15=
ENST00000442489.1:c.22C>A ENSP00000407597.1:p.Arg8=
ENST00000477087.1:n.155-943C>A
NM_004064.4:c.43C>A NP_004055.1:p.Arg15=
NM_004064.5:c.43C>A MANE Select NP_004055.1:p.Arg15=
Search 100 bp 5'
Search 100 bp 3'