Canonical Allele Identifier: CA383969771
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 582797
ClinVar RCV Id: RCV000706960 RCV002424721
dbSNP Id: rs767720666
gnomAD v2: 12-12871018-G-T
gnomAD v4: 12-12718084-G-T
MyVariant Identifiers: chr12:g.12871018G>T (hg19) chr12:g.12718084G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718084G>T , CM000674.2:g.12718084G>T GRCh38
NC_000012.11:g.12871018G>T , CM000674.1:g.12871018G>T GRCh37
NC_000012.10:g.12762285G>T NCBI36
NG_016341.1:g.5717G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.245G>T ENSP00000507272.1:p.Gly82Val
ENST00000682620.1:n.1631-741G>T
ENST00000684771.1:n.585-741G>T
ENST00000228872.9:c.245G>T MANE Select ENSP00000228872.4:p.Gly82Val
ENST00000228872.8:c.245G>T ENSP00000228872.4:p.Gly82Val
ENST00000396340.1:c.245G>T ENSP00000379629.1:p.Gly82Val
ENST00000442489.1:c.193+31G>T ENSP00000407597.1:n.193+31G>T
ENST00000477087.1:n.155-741G>T
NM_004064.4:c.245G>T NP_004055.1:p.Gly82Val
NM_004064.5:c.245G>T MANE Select NP_004055.1:p.Gly82Val
Search 100 bp 5'
Search 100 bp 3'