Canonical Allele Identifier: CA478845628

Gene: CDKN1B

Linked Data

• MyVariant Identifiers: chr12:g.12870980C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718046C>G , CM000674.2:g.12718046C>G	GRCh38
NC_000012.11:g.12870980C>G , CM000674.1:g.12870980C>G	GRCh37
NC_000012.10:g.12762247C>G	NCBI36
NG_016341.1:g.5679C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.207C>G	ENSP00000507272.1:p.Pro69=
ENST00000682620.1:n.1631-779C>G
ENST00000684771.1:n.585-779C>G
ENST00000228872.9:c.207C>G MANE Select	ENSP00000228872.4:p.Pro69=
ENST00000228872.8:c.207C>G	ENSP00000228872.4:p.Pro69=
ENST00000396340.1:c.207C>G	ENSP00000379629.1:p.Pro69=
ENST00000442489.1:c.186C>G	ENSP00000407597.1:p.Pro62=
ENST00000477087.1:n.155-779C>G
NM_004064.4:c.207C>G	NP_004055.1:p.Pro69=
NM_004064.5:c.207C>G MANE Select	NP_004055.1:p.Pro69=