Canonical Allele Identifier: CA383970206

Gene: CDKN1B

Linked Data

• dbSNP Id: rs2136356131
• COSMIC: COSM3398515
• MyVariant Identifiers: chr12:g.12871093A>G (hg19) ; chr12:g.12718159A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718159A>G , CM000674.2:g.12718159A>G	GRCh38
NC_000012.11:g.12871093A>G , CM000674.1:g.12871093A>G	GRCh37
NC_000012.10:g.12762360A>G	NCBI36
NG_016341.1:g.5792A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.320A>G	ENSP00000507272.1:p.Gln107Arg
ENST00000682620.1:n.1631-666A>G
ENST00000684771.1:n.585-666A>G
ENST00000228872.9:c.320A>G MANE Select	ENSP00000228872.4:p.Gln107Arg
ENST00000228872.8:c.320A>G	ENSP00000228872.4:p.Gln107Arg
ENST00000396340.1:c.320A>G	ENSP00000379629.1:p.Gln107Arg
ENST00000442489.1:c.193+106A>G	ENSP00000407597.1:n.193+106A>G
ENST00000477087.1:n.155-666A>G
NM_004064.4:c.320A>G	NP_004055.1:p.Gln107Arg
NM_004064.5:c.320A>G MANE Select	NP_004055.1:p.Gln107Arg