Canonical Allele Identifier: CA6457397
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 469001
ClinVar RCV Id: RCV000547886 RCV000567439 RCV003151786 RCV003935474
dbSNP Id: rs543122580
ExAC: 12:12870928 T / G
gnomAD v2: 12-12870928-T-G
gnomAD v3: 12-12717994-T-G
gnomAD v4: 12-12717994-T-G
MyVariant Identifiers: chr12:g.12870928T>G (hg19) chr12:g.12717994T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717994T>G , CM000674.2:g.12717994T>G GRCh38
NC_000012.11:g.12870928T>G , CM000674.1:g.12870928T>G GRCh37
NC_000012.10:g.12762195T>G NCBI36
NG_016341.1:g.5627T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.155T>G ENSP00000507272.1:p.Met52Arg
ENST00000682620.1:n.1631-831T>G
ENST00000684771.1:n.585-831T>G
ENST00000228872.9:c.155T>G MANE Select ENSP00000228872.4:p.Met52Arg
ENST00000228872.8:c.155T>G ENSP00000228872.4:p.Met52Arg
ENST00000396340.1:c.155T>G ENSP00000379629.1:p.Met52Arg
ENST00000442489.1:c.134T>G ENSP00000407597.1:p.Met45Arg
ENST00000477087.1:n.155-831T>G
NM_004064.4:c.155T>G NP_004055.1:p.Met52Arg
NM_004064.5:c.155T>G MANE Select NP_004055.1:p.Met52Arg
Search 100 bp 5'
Search 100 bp 3'