Canonical Allele Identifier: CA2017047114

Gene: CDKN1B GPR19

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717398A= , CM000674.2:g.12717398A=	GRCh38
NC_000012.11:g.12870332A= , CM000674.1:g.12870332A=	GRCh37
NC_000012.10:g.12761599A=	NCBI36
NG_016341.1:g.5031A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-442A= (CDKN1B)	ENSP00000507272.1:n.-442A=
ENST00000682620.1:n.1631-1427A= (CDKN1B)
ENST00000684771.1:n.585-1427A= (CDKN1B)
ENST00000228872.9:c.-442A= (CDKN1B) MANE Select	ENSP00000228872.4:n.-442A=
ENST00000228872.8:c.-442A= (CDKN1B)	ENSP00000228872.4:n.-442A=
ENST00000477087.1:n.155-1427A= (CDKN1B)
NM_004064.4:c.-442A= (CDKN1B)	NP_004055.1:n.-442A=
XM_011520623.3:c.-1892T= (GPR19)	XP_011518925.1:n.-1892T=
XM_017019216.2:c.-1920T= (GPR19)	XP_016874705.1:n.-1920T=
NM_004064.5:c.-442A= (CDKN1B) MANE Select	NP_004055.1:n.-442A=