Canonical Allele Identifier: CA383969375

Gene: CDKN1B

Linked Data

• MyVariant Identifiers: chr12:g.12870964T>A (hg19) ; chr12:g.12718030T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718030T>A , CM000674.2:g.12718030T>A	GRCh38
NC_000012.11:g.12870964T>A , CM000674.1:g.12870964T>A	GRCh37
NC_000012.10:g.12762231T>A	NCBI36
NG_016341.1:g.5663T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000614874.2:c.191T>A	ENSP00000507272.1:p.Phe64Tyr
ENST00000682620.1:n.1631-795T>A
ENST00000684771.1:n.585-795T>A
ENST00000228872.9:c.191T>A MANE Select	ENSP00000228872.4:p.Phe64Tyr
ENST00000228872.8:c.191T>A	ENSP00000228872.4:p.Phe64Tyr
ENST00000396340.1:c.191T>A	ENSP00000379629.1:p.Phe64Tyr
ENST00000442489.1:c.170T>A	ENSP00000407597.1:p.Phe57Tyr
ENST00000477087.1:n.155-795T>A
NM_004064.4:c.191T>A	NP_004055.1:p.Phe64Tyr
NM_004064.5:c.191T>A MANE Select	NP_004055.1:p.Phe64Tyr