Canonical Allele Identifier: CA6457368

Gene: CDKN1B

Linked Data

• ClinVar Variation Id: 704812
• ClinVar RCV Id: RCV001022243 ; RCV000874995
• dbSNP Id: rs747456770
• ExAC: 12:12870815 G / A
• gnomAD v2: 12-12870815-G-A
• gnomAD v4: 12-12717881-G-A
• MyVariant Identifiers: chr12:g.12870815G>A (hg19) ; chr12:g.12717881G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717881G>A , CM000674.2:g.12717881G>A	GRCh38
NC_000012.11:g.12870815G>A , CM000674.1:g.12870815G>A	GRCh37
NC_000012.10:g.12762082G>A	NCBI36
NG_016341.1:g.5514G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.42G>A	ENSP00000507272.1:p.Glu14=
ENST00000682620.1:n.1631-944G>A
ENST00000684771.1:n.585-944G>A
ENST00000228872.9:c.42G>A MANE Select	ENSP00000228872.4:p.Glu14=
ENST00000228872.8:c.42G>A	ENSP00000228872.4:p.Glu14=
ENST00000396340.1:c.42G>A	ENSP00000379629.1:p.Glu14=
ENST00000442489.1:c.21G>A	ENSP00000407597.1:p.Glu7=
ENST00000477087.1:n.155-944G>A
NM_004064.4:c.42G>A	NP_004055.1:p.Glu14=
NM_004064.5:c.42G>A MANE Select	NP_004055.1:p.Glu14=