Canonical Allele Identifier: CA2017047150

Gene: CDKN1B GPR19

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717438T= , CM000674.2:g.12717438T=	GRCh38
NC_000012.11:g.12870372T= , CM000674.1:g.12870372T=	GRCh37
NC_000012.10:g.12761639T=	NCBI36
NG_016341.1:g.5071T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-402T= (CDKN1B)	ENSP00000507272.1:n.-402T=
ENST00000682620.1:n.1631-1387T= (CDKN1B)
ENST00000684771.1:n.585-1387T= (CDKN1B)
ENST00000228872.9:c.-402T= (CDKN1B) MANE Select	ENSP00000228872.4:n.-402T=
ENST00000228872.8:c.-402T= (CDKN1B)	ENSP00000228872.4:n.-402T=
ENST00000477087.1:n.155-1387T= (CDKN1B)
NM_004064.4:c.-402T= (CDKN1B)	NP_004055.1:n.-402T=
XM_011520623.3:c.-1932A= (GPR19)	XP_011518925.1:n.-1932A=
XM_017019216.2:c.-1960A= (GPR19)	XP_016874705.1:n.-1960A=
NM_004064.5:c.-402T= (CDKN1B) MANE Select	NP_004055.1:n.-402T=