Canonical Allele Identifier: CA478845849
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1624753
ClinVar RCV Id: RCV002106339 RCV002325661
dbSNP Id: rs534581124
MyVariant Identifiers: chr12:g.12871184G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718250G>C , CM000674.2:g.12718250G>C GRCh38
NC_000012.11:g.12871184G>C , CM000674.1:g.12871184G>C GRCh37
NC_000012.10:g.12762451G>C NCBI36
NG_016341.1:g.5883G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.411G>C ENSP00000507272.1:p.Pro137=
ENST00000682620.1:n.1631-575G>C
ENST00000684771.1:n.585-575G>C
ENST00000228872.9:c.411G>C MANE Select ENSP00000228872.4:p.Pro137=
ENST00000228872.8:c.411G>C ENSP00000228872.4:p.Pro137=
ENST00000396340.1:c.411G>C ENSP00000379629.1:p.Pro137=
ENST00000442489.1:c.193+197G>C ENSP00000407597.1:n.193+197G>C
ENST00000477087.1:n.155-575G>C
NM_004064.4:c.411G>C NP_004055.1:p.Pro137=
NM_004064.5:c.411G>C MANE Select NP_004055.1:p.Pro137=
Search 100 bp 5'
Search 100 bp 3'