Canonical Allele Identifier: CA383968581

Gene: CDKN1B

Linked Data

• dbSNP Id: rs1946488422
• MyVariant Identifiers: chr12:g.12870873G>C (hg19) ; chr12:g.12717939G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717939G>C , CM000674.2:g.12717939G>C	GRCh38
NC_000012.11:g.12870873G>C , CM000674.1:g.12870873G>C	GRCh37
NC_000012.10:g.12762140G>C	NCBI36
NG_016341.1:g.5572G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000614874.2:c.100G>C	ENSP00000507272.1:p.Gly34Arg
ENST00000682620.1:n.1631-886G>C
ENST00000684771.1:n.585-886G>C
ENST00000228872.9:c.100G>C MANE Select	ENSP00000228872.4:p.Gly34Arg
ENST00000228872.8:c.100G>C	ENSP00000228872.4:p.Gly34Arg
ENST00000396340.1:c.100G>C	ENSP00000379629.1:p.Gly34Arg
ENST00000442489.1:c.79G>C	ENSP00000407597.1:p.Gly27Arg
ENST00000477087.1:n.155-886G>C
NM_004064.4:c.100G>C	NP_004055.1:p.Gly34Arg
NM_004064.5:c.100G>C MANE Select	NP_004055.1:p.Gly34Arg