Canonical Allele Identifier: CA383967985
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1498811
ClinVar RCV Id: RCV001999396
dbSNP Id: rs755225286
MyVariant Identifiers: chr12:g.12870798G>C (hg19) chr12:g.12717864G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717864G>C , CM000674.2:g.12717864G>C GRCh38
NC_000012.11:g.12870798G>C , CM000674.1:g.12870798G>C GRCh37
NC_000012.10:g.12762065G>C NCBI36
NG_016341.1:g.5497G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.25G>C ENSP00000507272.1:p.Gly9Arg
ENST00000682620.1:n.1631-961G>C
ENST00000684771.1:n.585-961G>C
ENST00000228872.9:c.25G>C MANE Select ENSP00000228872.4:p.Gly9Arg
ENST00000228872.8:c.25G>C ENSP00000228872.4:p.Gly9Arg
ENST00000396340.1:c.25G>C ENSP00000379629.1:p.Gly9Arg
ENST00000442489.1:c.4G>C ENSP00000407597.1:p.Gly2Arg
ENST00000477087.1:n.155-961G>C
NM_004064.4:c.25G>C NP_004055.1:p.Gly9Arg
NM_004064.5:c.25G>C MANE Select NP_004055.1:p.Gly9Arg
Search 100 bp 5'
Search 100 bp 3'