Canonical Allele Identifier: CA478846019
Gene: CDKN1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.12871238T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718304T>G , CM000674.2:g.12718304T>G GRCh38
NC_000012.11:g.12871238T>G , CM000674.1:g.12871238T>G GRCh37
NC_000012.10:g.12762505T>G NCBI36
NG_016341.1:g.5937T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.465T>G ENSP00000507272.1:p.Pro155=
ENST00000682620.1:n.1631-521T>G
ENST00000684771.1:n.585-521T>G
ENST00000228872.9:c.465T>G MANE Select ENSP00000228872.4:p.Pro155=
ENST00000228872.8:c.465T>G ENSP00000228872.4:p.Pro155=
ENST00000396340.1:c.465T>G ENSP00000379629.1:p.Pro155=
ENST00000442489.1:c.193+251T>G ENSP00000407597.1:n.193+251T>G
ENST00000477087.1:n.155-521T>G
NM_004064.4:c.465T>G NP_004055.1:p.Pro155=
NM_004064.5:c.465T>G MANE Select NP_004055.1:p.Pro155=
Search 100 bp 5'
Search 100 bp 3'