Canonical Allele Identifier: CA1595296869

Gene: ADRA1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159924377T= , CM000667.2:g.159924377T=	GRCh38
NC_000005.9:g.159351384T= , CM000667.1:g.159351384T=	GRCh37
NC_000005.8:g.159283962T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306675.5:c.949+6523T= MANE Select	ENSP00000306662.3:n.949+6523T=
ENST00000306675.3:c.949+6523T=	ENSP00000306662.3:n.949+6523T=
NM_000679.3:c.949+6523T=	NP_000670.1:n.949+6523T=
XM_005265818.2:c.949+6523T=	XP_005265875.1:n.949+6523T=
XM_005265819.2:c.949+6523T=	XP_005265876.1:n.949+6523T=
XM_006714821.2:c.949+6523T=	XP_006714884.1:n.949+6523T=
XM_011534435.1:c.950-1112T=	XP_011532737.1:n.950-1112T=
XM_011534436.1:c.950-1112T=	XP_011532738.1:n.950-1112T=
XM_011534437.1:c.950-1112T=	XP_011532739.1:n.950-1112T=
XM_011534438.1:c.950-1112T=	XP_011532740.1:n.950-1112T=
XM_011534439.1:c.950-1112T=	XP_011532741.1:n.950-1112T=
XM_011534440.1:c.950-1112T=	XP_011532742.1:n.950-1112T=
XM_005265818.3:c.949+6523T=	XP_005265875.1:n.949+6523T=
XM_006714821.3:c.949+6523T=	XP_006714884.1:n.949+6523T=
XM_011534437.2:c.950-1112T=	XP_011532739.1:n.950-1112T=
XM_011534438.2:c.950-1112T=	XP_011532740.1:n.950-1112T=
NM_000679.4:c.949+6523T= MANE Select	NP_000670.1:n.949+6523T=