Canonical Allele Identifier: CA383969874

Gene: CDKN1B

Linked Data

• MyVariant Identifiers: chr12:g.12871036A>G (hg19) ; chr12:g.12718102A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718102A>G , CM000674.2:g.12718102A>G	GRCh38
NC_000012.11:g.12871036A>G , CM000674.1:g.12871036A>G	GRCh37
NC_000012.10:g.12762303A>G	NCBI36
NG_016341.1:g.5735A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000614874.2:c.263A>G	ENSP00000507272.1:p.Tyr88Cys
ENST00000682620.1:n.1631-723A>G
ENST00000684771.1:n.585-723A>G
ENST00000228872.9:c.263A>G MANE Select	ENSP00000228872.4:p.Tyr88Cys
ENST00000228872.8:c.263A>G	ENSP00000228872.4:p.Tyr88Cys
ENST00000396340.1:c.263A>G	ENSP00000379629.1:p.Tyr88Cys
ENST00000442489.1:c.193+49A>G	ENSP00000407597.1:n.193+49A>G
ENST00000477087.1:n.155-723A>G
NM_004064.4:c.263A>G	NP_004055.1:p.Tyr88Cys
NM_004064.5:c.263A>G MANE Select	NP_004055.1:p.Tyr88Cys