Canonical Allele Identifier: CA1595315767

Gene: ADRA1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159937821C= , CM000667.2:g.159937821C=	GRCh38
NC_000005.9:g.159364828C= , CM000667.1:g.159364828C=	GRCh37
NC_000005.8:g.159297406C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+19967C= MANE Select	ENSP00000306662.3:n.949+19967C=
ENST00000306675.3:c.949+19967C=	ENSP00000306662.3:n.949+19967C=
NM_000679.3:c.949+19967C=	NP_000670.1:n.949+19967C=
XM_005265818.2:c.950-9869C=	XP_005265875.1:n.950-9869C=
XM_005265819.2:c.950-17292C=	XP_005265876.1:n.950-17292C=
XM_006714821.2:c.949+19967C=	XP_006714884.1:n.949+19967C=
XM_011534435.1:c.1057+12225C=	XP_011532737.1:n.1057+12225C=
XM_011534436.1:c.1057+12225C=	XP_011532738.1:n.1057+12225C=
XM_011534437.1:c.1058-9869C=	XP_011532739.1:n.1058-9869C=
XM_011534439.1:c.1057+12225C=	XP_011532741.1:n.1057+12225C=
XM_005265818.3:c.950-9869C=	XP_005265875.1:n.950-9869C=
XM_006714821.3:c.949+19967C=	XP_006714884.1:n.949+19967C=
XM_011534437.2:c.1058-9869C=	XP_011532739.1:n.1058-9869C=
XR_001742950.1:n.3797G=
NM_000679.4:c.949+19967C= MANE Select	NP_000670.1:n.949+19967C=