Canonical Allele Identifier: CA2769128855

Gene: ADRA1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159921542C>A , CM000667.2:g.159921542C>A	GRCh38
NC_000005.9:g.159348549C>A , CM000667.1:g.159348549C>A	GRCh37
NC_000005.8:g.159281127C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+3688C>A MANE Select	ENSP00000306662.3:n.949+3688C>A
ENST00000306675.3:c.949+3688C>A	ENSP00000306662.3:n.949+3688C>A
NM_000679.3:c.949+3688C>A	NP_000670.1:n.949+3688C>A
XM_005265818.2:c.949+3688C>A	XP_005265875.1:n.949+3688C>A
XM_005265819.2:c.949+3688C>A	XP_005265876.1:n.949+3688C>A
XM_006714821.2:c.949+3688C>A	XP_006714884.1:n.949+3688C>A
XM_011534435.1:c.949+3688C>A	XP_011532737.1:n.949+3688C>A
XM_011534436.1:c.949+3688C>A	XP_011532738.1:n.949+3688C>A
XM_011534437.1:c.949+3688C>A	XP_011532739.1:n.949+3688C>A
XM_011534438.1:c.949+3688C>A	XP_011532740.1:n.949+3688C>A
XM_011534439.1:c.949+3688C>A	XP_011532741.1:n.949+3688C>A
XM_011534440.1:c.949+3688C>A	XP_011532742.1:n.949+3688C>A
XM_005265818.3:c.949+3688C>A	XP_005265875.1:n.949+3688C>A
XM_006714821.3:c.949+3688C>A	XP_006714884.1:n.949+3688C>A
XM_011534437.2:c.949+3688C>A	XP_011532739.1:n.949+3688C>A
XM_011534438.2:c.949+3688C>A	XP_011532740.1:n.949+3688C>A
NM_000679.4:c.949+3688C>A MANE Select	NP_000670.1:n.949+3688C>A