Canonical Allele Identifier: CA478845977
Gene: CDKN1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.12871223A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718289A>C , CM000674.2:g.12718289A>C GRCh38
NC_000012.11:g.12871223A>C , CM000674.1:g.12871223A>C GRCh37
NC_000012.10:g.12762490A>C NCBI36
NG_016341.1:g.5922A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.450A>C ENSP00000507272.1:p.Gly150=
ENST00000682620.1:n.1631-536A>C
ENST00000684771.1:n.585-536A>C
ENST00000228872.9:c.450A>C MANE Select ENSP00000228872.4:p.Gly150=
ENST00000228872.8:c.450A>C ENSP00000228872.4:p.Gly150=
ENST00000396340.1:c.450A>C ENSP00000379629.1:p.Gly150=
ENST00000442489.1:c.193+236A>C ENSP00000407597.1:n.193+236A>C
ENST00000477087.1:n.155-536A>C
NM_004064.4:c.450A>C NP_004055.1:p.Gly150=
NM_004064.5:c.450A>C MANE Select NP_004055.1:p.Gly150=
Search 100 bp 5'
Search 100 bp 3'