Canonical Allele Identifier: CA478845505

Gene: CDKN1B

Linked Data

• MyVariant Identifiers: chr12:g.12870896A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717962A>G , CM000674.2:g.12717962A>G	GRCh38
NC_000012.11:g.12870896A>G , CM000674.1:g.12870896A>G	GRCh37
NC_000012.10:g.12762163A>G	NCBI36
NG_016341.1:g.5595A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.123A>G	ENSP00000507272.1:p.Leu41=
ENST00000682620.1:n.1631-863A>G
ENST00000684771.1:n.585-863A>G
ENST00000228872.9:c.123A>G MANE Select	ENSP00000228872.4:p.Leu41=
ENST00000228872.8:c.123A>G	ENSP00000228872.4:p.Leu41=
ENST00000396340.1:c.123A>G	ENSP00000379629.1:p.Leu41=
ENST00000442489.1:c.102A>G	ENSP00000407597.1:p.Leu34=
ENST00000477087.1:n.155-863A>G
NM_004064.4:c.123A>G	NP_004055.1:p.Leu41=
NM_004064.5:c.123A>G MANE Select	NP_004055.1:p.Leu41=