Canonical Allele Identifier: CA2017047308
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717626T= , CM000674.2:g.12717626T= GRCh38
NC_000012.11:g.12870560T= , CM000674.1:g.12870560T= GRCh37
NC_000012.10:g.12761827T= NCBI36
NG_016341.1:g.5259T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.-214T= (CDKN1B) ENSP00000507272.1:n.-214T=
ENST00000682620.1:n.1631-1199T= (CDKN1B)
ENST00000684771.1:n.585-1199T= (CDKN1B)
ENST00000228872.9:c.-214T= (CDKN1B) MANE Select ENSP00000228872.4:n.-214T=
ENST00000228872.8:c.-214T= (CDKN1B) ENSP00000228872.4:n.-214T=
ENST00000477087.1:n.155-1199T= (CDKN1B)
NM_004064.4:c.-214T= (CDKN1B) NP_004055.1:n.-214T=
XM_011520623.3:c.-2120A= (GPR19) XP_011518925.1:n.-2120A=
XM_017019216.2:c.-2148A= (GPR19) XP_016874705.1:n.-2148A=
NM_004064.5:c.-214T= (CDKN1B) MANE Select NP_004055.1:n.-214T=