Canonical Allele Identifier: CA478845412
Gene: CDKN1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.12870857C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717923C>G , CM000674.2:g.12717923C>G GRCh38
NC_000012.11:g.12870857C>G , CM000674.1:g.12870857C>G GRCh37
NC_000012.10:g.12762124C>G NCBI36
NG_016341.1:g.5556C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.84C>G ENSP00000507272.1:p.Ala28=
ENST00000682620.1:n.1631-902C>G
ENST00000684771.1:n.585-902C>G
ENST00000228872.9:c.84C>G MANE Select ENSP00000228872.4:p.Ala28=
ENST00000228872.8:c.84C>G ENSP00000228872.4:p.Ala28=
ENST00000396340.1:c.84C>G ENSP00000379629.1:p.Ala28=
ENST00000442489.1:c.63C>G ENSP00000407597.1:p.Ala21=
ENST00000477087.1:n.155-902C>G
NM_004064.4:c.84C>G NP_004055.1:p.Ala28=
NM_004064.5:c.84C>G MANE Select NP_004055.1:p.Ala28=