Canonical Allele Identifier: CA684981689

Gene: CDKN1B

Linked Data

• dbSNP Id: rs1158620228
• gnomAD v3: 12-12718631-GC-G
• gnomAD v4: 12-12718631-GC-G
• MyVariant Identifiers: chr12:g.12871566del (hg19) ; chr12:g.12718632del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718632del , CM000674.2:g.12718632del	GRCh38
NC_000012.11:g.12871566del , CM000674.1:g.12871566del	GRCh37
NC_000012.10:g.12762833del	NCBI36
NG_016341.1:g.6265del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.476-193del	ENSP00000507272.1:n.476-193del
ENST00000682620.1:n.1631-193del
ENST00000684771.1:n.585-193del
ENST00000228872.9:c.476-193del MANE Select	ENSP00000228872.4:n.476-193del
ENST00000228872.8:c.476-193del	ENSP00000228872.4:n.476-193del
ENST00000396340.1:c.475+318del	ENSP00000379629.1:n.475+318del
ENST00000442489.1:c.194-193del	ENSP00000407597.1:n.194-193del
ENST00000477087.1:n.155-193del
NM_004064.4:c.476-193del	NP_004055.1:n.476-193del
NM_004064.5:c.476-193del MANE Select	NP_004055.1:n.476-193del