Canonical Allele Identifier: CA1595301830

Gene: ADRA1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159933331C= , CM000667.2:g.159933331C=	GRCh38
NC_000005.9:g.159360338C= , CM000667.1:g.159360338C=	GRCh37
NC_000005.8:g.159292916C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+15477C= MANE Select	ENSP00000306662.3:n.949+15477C=
ENST00000306675.3:c.949+15477C=	ENSP00000306662.3:n.949+15477C=
NM_000679.3:c.949+15477C=	NP_000670.1:n.949+15477C=
XM_005265818.2:c.950-14359C=	XP_005265875.1:n.950-14359C=
XM_005265819.2:c.949+15477C=	XP_005265876.1:n.949+15477C=
XM_006714821.2:c.949+15477C=	XP_006714884.1:n.949+15477C=
XM_011534435.1:c.1057+7735C=	XP_011532737.1:n.1057+7735C=
XM_011534436.1:c.1057+7735C=	XP_011532738.1:n.1057+7735C=
XM_011534437.1:c.1057+7735C=	XP_011532739.1:n.1057+7735C=
XM_011534439.1:c.1057+7735C=	XP_011532741.1:n.1057+7735C=
XM_005265818.3:c.950-14359C=	XP_005265875.1:n.950-14359C=
XM_006714821.3:c.949+15477C=	XP_006714884.1:n.949+15477C=
XM_011534437.2:c.1057+7735C=	XP_011532739.1:n.1057+7735C=
NM_000679.4:c.949+15477C= MANE Select	NP_000670.1:n.949+15477C=