Canonical Allele Identifier: CA383968539

Gene: CDKN1B

Linked Data

• MyVariant Identifiers: chr12:g.12870871T>A (hg19) ; chr12:g.12717937T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717937T>A , CM000674.2:g.12717937T>A	GRCh38
NC_000012.11:g.12870871T>A , CM000674.1:g.12870871T>A	GRCh37
NC_000012.10:g.12762138T>A	NCBI36
NG_016341.1:g.5570T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000614874.2:c.98T>A	ENSP00000507272.1:p.Phe33Tyr
ENST00000682620.1:n.1631-888T>A
ENST00000684771.1:n.585-888T>A
ENST00000228872.9:c.98T>A MANE Select	ENSP00000228872.4:p.Phe33Tyr
ENST00000228872.8:c.98T>A	ENSP00000228872.4:p.Phe33Tyr
ENST00000396340.1:c.98T>A	ENSP00000379629.1:p.Phe33Tyr
ENST00000442489.1:c.77T>A	ENSP00000407597.1:p.Phe26Tyr
ENST00000477087.1:n.155-888T>A
NM_004064.4:c.98T>A	NP_004055.1:p.Phe33Tyr
NM_004064.5:c.98T>A MANE Select	NP_004055.1:p.Phe33Tyr