Canonical Allele Identifier: CA478845936

Gene: CDKN1B

Linked Data

• ClinVar Variation Id: 1740210
• ClinVar RCV Id: RCV002333629 ; RCV003619770
• dbSNP Id: rs2136356542
• COSMIC: COSM5783787
• MyVariant Identifiers: chr12:g.12871211G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718277G>A , CM000674.2:g.12718277G>A	GRCh38
NC_000012.11:g.12871211G>A , CM000674.1:g.12871211G>A	GRCh37
NC_000012.10:g.12762478G>A	NCBI36
NG_016341.1:g.5910G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.438G>A	ENSP00000507272.1:p.Glu146=
ENST00000682620.1:n.1631-548G>A
ENST00000684771.1:n.585-548G>A
ENST00000228872.9:c.438G>A MANE Select	ENSP00000228872.4:p.Glu146=
ENST00000228872.8:c.438G>A	ENSP00000228872.4:p.Glu146=
ENST00000396340.1:c.438G>A	ENSP00000379629.1:p.Glu146=
ENST00000442489.1:c.193+224G>A	ENSP00000407597.1:n.193+224G>A
ENST00000477087.1:n.155-548G>A
NM_004064.4:c.438G>A	NP_004055.1:p.Glu146=
NM_004064.5:c.438G>A MANE Select	NP_004055.1:p.Glu146=