Canonical Allele Identifier: CA603358573

Gene: CDKN1B

Linked Data

• gnomAD v2: 12-12871549-G-C
• MyVariant Identifiers: chr12:g.12871549G>C (hg19) ; chr12:g.12718615G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718615G>C , CM000674.2:g.12718615G>C	GRCh38
NC_000012.11:g.12871549G>C , CM000674.1:g.12871549G>C	GRCh37
NC_000012.10:g.12762816G>C	NCBI36
NG_016341.1:g.6248G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.476-210G>C	ENSP00000507272.1:n.476-210G>C
ENST00000682620.1:n.1631-210G>C
ENST00000684771.1:n.585-210G>C
ENST00000228872.9:c.476-210G>C MANE Select	ENSP00000228872.4:n.476-210G>C
ENST00000228872.8:c.476-210G>C	ENSP00000228872.4:n.476-210G>C
ENST00000396340.1:c.475+301G>C	ENSP00000379629.1:n.475+301G>C
ENST00000442489.1:c.194-210G>C	ENSP00000407597.1:n.194-210G>C
ENST00000477087.1:n.155-210G>C
NM_004064.4:c.476-210G>C	NP_004055.1:n.476-210G>C
NM_004064.5:c.476-210G>C MANE Select	NP_004055.1:n.476-210G>C