Canonical Allele Identifier: CA2017047926
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs1946503415

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718451_12718452insTT , CM000674.2:g.12718451_12718452insTT GRCh38
NC_000012.11:g.12871385_12871386insTT , CM000674.1:g.12871385_12871386insTT GRCh37
NC_000012.10:g.12762652_12762653insTT NCBI36
NG_016341.1:g.6084_6085insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.475+137_475+138insTT ENSP00000507272.1:n.475+137_475+138insTT
ENST00000682620.1:n.1631-374_1631-373insTT
ENST00000684771.1:n.585-374_585-373insTT
ENST00000228872.9:c.475+137_475+138insTT MANE Select ENSP00000228872.4:n.475+137_475+138insTT
ENST00000228872.8:c.475+137_475+138insTT ENSP00000228872.4:n.475+137_475+138insTT
ENST00000396340.1:c.475+137_475+138insTT ENSP00000379629.1:n.475+137_475+138insTT
ENST00000442489.1:c.194-374_194-373insTT ENSP00000407597.1:n.194-374_194-373insTT
ENST00000477087.1:n.155-374_155-373insTT
NM_004064.4:c.475+137_475+138insTT NP_004055.1:n.475+137_475+138insTT
NM_004064.5:c.475+137_475+138insTT MANE Select NP_004055.1:n.475+137_475+138insTT