Canonical Allele Identifier: CA1595317243
Gene: ADRA1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159941018G= , CM000667.2:g.159941018G= GRCh38
NC_000005.9:g.159368025G= , CM000667.1:g.159368025G= GRCh37
NC_000005.8:g.159300603G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306675.5:c.949+23164G= MANE Select ENSP00000306662.3:n.949+23164G=
ENST00000306675.3:c.949+23164G= ENSP00000306662.3:n.949+23164G=
NM_000679.3:c.949+23164G= NP_000670.1:n.949+23164G=
XM_005265818.2:c.950-6672G= XP_005265875.1:n.950-6672G=
XM_005265819.2:c.950-14095G= XP_005265876.1:n.950-14095G=
XM_006714821.2:c.949+23164G= XP_006714884.1:n.949+23164G=
XM_011534435.1:c.1057+15422G= XP_011532737.1:n.1057+15422G=
XM_011534436.1:c.1058-14082G= XP_011532738.1:n.1058-14082G=
XM_011534437.1:c.1058-6672G= XP_011532739.1:n.1058-6672G=
XM_011534439.1:c.1058-14095G= XP_011532741.1:n.1058-14095G=
XM_005265818.3:c.950-6672G= XP_005265875.1:n.950-6672G=
XM_006714821.3:c.949+23164G= XP_006714884.1:n.949+23164G=
XM_011534437.2:c.1058-6672G= XP_011532739.1:n.1058-6672G=
XR_001742950.1:n.600C=
NM_000679.4:c.949+23164G= MANE Select NP_000670.1:n.949+23164G=