Canonical Allele Identifier: CA684981659

Gene: CDKN1B

Linked Data

• dbSNP Id: rs1261378989
• MyVariant Identifiers: chr12:g.12871508G>A (hg19) ; chr12:g.12718574G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718574G>A , CM000674.2:g.12718574G>A	GRCh38
NC_000012.11:g.12871508G>A , CM000674.1:g.12871508G>A	GRCh37
NC_000012.10:g.12762775G>A	NCBI36
NG_016341.1:g.6207G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.476-251G>A	ENSP00000507272.1:n.476-251G>A
ENST00000682620.1:n.1631-251G>A
ENST00000684771.1:n.585-251G>A
ENST00000228872.9:c.476-251G>A MANE Select	ENSP00000228872.4:n.476-251G>A
ENST00000228872.8:c.476-251G>A	ENSP00000228872.4:n.476-251G>A
ENST00000396340.1:c.475+260G>A	ENSP00000379629.1:n.475+260G>A
ENST00000442489.1:c.194-251G>A	ENSP00000407597.1:n.194-251G>A
ENST00000477087.1:n.155-251G>A
NM_004064.4:c.476-251G>A	NP_004055.1:n.476-251G>A
NM_004064.5:c.476-251G>A MANE Select	NP_004055.1:n.476-251G>A