Canonical Allele Identifier: CA1630855537

Gene: CDKN1B GPR19

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717761T= , CM000674.2:g.12717761T=	GRCh38
NC_000012.11:g.12870695T= , CM000674.1:g.12870695T=	GRCh37
NC_000012.10:g.12761962T=	NCBI36
NG_016341.1:g.5394T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004064.5:c.-79T= (CDKN1B) MANE Select	NP_004055.1:n.-79T=
ENST00000228872.9:c.-79T= (CDKN1B) MANE Select	ENSP00000228872.4:n.-79T=
NM_004064.4:c.-79T= (CDKN1B)	NP_004055.1:n.-79T=
ENST00000228872.8:c.-79T= (CDKN1B)	ENSP00000228872.4:n.-79T=
ENST00000477087.1:n.155-1064T= (CDKN1B)
ENST00000614874.2:c.-79T= (CDKN1B)	ENSP00000507272.1:n.-79T=
ENST00000682620.1:n.1631-1064T= (CDKN1B)
ENST00000684771.1:n.585-1064T= (CDKN1B)
XM_011520623.3:c.-2255A= (GPR19)	XP_011518925.1:n.-2255A=
XM_017019216.2:c.-2283A= (GPR19)	XP_016874705.1:n.-2283A=