Canonical Allele Identifier: CA944840890
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs1946507641
gnomAD v3: 12-12718675-G-A
gnomAD v4: 12-12718675-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718675G>A , CM000674.2:g.12718675G>A GRCh38
NC_000012.11:g.12871609G>A , CM000674.1:g.12871609G>A GRCh37
NC_000012.10:g.12762876G>A NCBI36
NG_016341.1:g.6308G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.476-150G>A ENSP00000507272.1:n.476-150G>A
ENST00000682620.1:n.1631-150G>A
ENST00000684771.1:n.585-150G>A
ENST00000228872.9:c.476-150G>A MANE Select ENSP00000228872.4:n.476-150G>A
ENST00000228872.8:c.476-150G>A ENSP00000228872.4:n.476-150G>A
ENST00000396340.1:c.475+361G>A ENSP00000379629.1:n.475+361G>A
ENST00000442489.1:c.194-150G>A ENSP00000407597.1:n.194-150G>A
ENST00000477087.1:n.155-150G>A
NM_004064.4:c.476-150G>A NP_004055.1:n.476-150G>A
NM_004064.5:c.476-150G>A MANE Select NP_004055.1:n.476-150G>A
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