Canonical Allele Identifier: CA383968611

Gene: CDKN1B

Linked Data

• ClinVar Variation Id: 1026814
• ClinVar RCV Id: RCV001327314
• dbSNP Id: rs1946488503
• MyVariant Identifiers: chr12:g.12870876C>G (hg19) ; chr12:g.12717942C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717942C>G , CM000674.2:g.12717942C>G	GRCh38
NC_000012.11:g.12870876C>G , CM000674.1:g.12870876C>G	GRCh37
NC_000012.10:g.12762143C>G	NCBI36
NG_016341.1:g.5575C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.103C>G	ENSP00000507272.1:p.Pro35Ala
ENST00000682620.1:n.1631-883C>G
ENST00000684771.1:n.585-883C>G
ENST00000228872.9:c.103C>G MANE Select	ENSP00000228872.4:p.Pro35Ala
ENST00000228872.8:c.103C>G	ENSP00000228872.4:p.Pro35Ala
ENST00000396340.1:c.103C>G	ENSP00000379629.1:p.Pro35Ala
ENST00000442489.1:c.82C>G	ENSP00000407597.1:p.Pro28Ala
ENST00000477087.1:n.155-883C>G
NM_004064.4:c.103C>G	NP_004055.1:p.Pro35Ala
NM_004064.5:c.103C>G MANE Select	NP_004055.1:p.Pro35Ala