Canonical Allele Identifier: CA2017047117
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717401G= , CM000674.2:g.12717401G= GRCh38
NC_000012.11:g.12870335G= , CM000674.1:g.12870335G= GRCh37
NC_000012.10:g.12761602G= NCBI36
NG_016341.1:g.5034G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.-439G= (CDKN1B) ENSP00000507272.1:n.-439G=
ENST00000682620.1:n.1631-1424G= (CDKN1B)
ENST00000684771.1:n.585-1424G= (CDKN1B)
ENST00000228872.9:c.-439G= (CDKN1B) MANE Select ENSP00000228872.4:n.-439G=
ENST00000228872.8:c.-439G= (CDKN1B) ENSP00000228872.4:n.-439G=
ENST00000477087.1:n.155-1424G= (CDKN1B)
NM_004064.4:c.-439G= (CDKN1B) NP_004055.1:n.-439G=
XM_011520623.3:c.-1895C= (GPR19) XP_011518925.1:n.-1895C=
XM_017019216.2:c.-1923C= (GPR19) XP_016874705.1:n.-1923C=
NM_004064.5:c.-439G= (CDKN1B) MANE Select NP_004055.1:n.-439G=