Canonical Allele Identifier: CA383970063

Gene: CDKN1B

Linked Data

• ClinVar Variation Id: 2450787
• ClinVar RCV Id: RCV003177204
• MyVariant Identifiers: chr12:g.12871063G>A (hg19) ; chr12:g.12718129G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718129G>A , CM000674.2:g.12718129G>A	GRCh38
NC_000012.11:g.12871063G>A , CM000674.1:g.12871063G>A	GRCh37
NC_000012.10:g.12762330G>A	NCBI36
NG_016341.1:g.5762G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000614874.2:c.290G>A	ENSP00000507272.1:p.Gly97Asp
ENST00000682620.1:n.1631-696G>A
ENST00000684771.1:n.585-696G>A
ENST00000228872.9:c.290G>A MANE Select	ENSP00000228872.4:p.Gly97Asp
ENST00000228872.8:c.290G>A	ENSP00000228872.4:p.Gly97Asp
ENST00000396340.1:c.290G>A	ENSP00000379629.1:p.Gly97Asp
ENST00000442489.1:c.193+76G>A	ENSP00000407597.1:n.193+76G>A
ENST00000477087.1:n.155-696G>A
NM_004064.4:c.290G>A	NP_004055.1:p.Gly97Asp
NM_004064.5:c.290G>A MANE Select	NP_004055.1:p.Gly97Asp