Canonical Allele Identifier: CA1595317245
Gene: ADRA1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159941021G= , CM000667.2:g.159941021G= GRCh38
NC_000005.9:g.159368028G= , CM000667.1:g.159368028G= GRCh37
NC_000005.8:g.159300606G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306675.5:c.949+23167G= MANE Select ENSP00000306662.3:n.949+23167G=
ENST00000306675.3:c.949+23167G= ENSP00000306662.3:n.949+23167G=
NM_000679.3:c.949+23167G= NP_000670.1:n.949+23167G=
XM_005265818.2:c.950-6669G= XP_005265875.1:n.950-6669G=
XM_005265819.2:c.950-14092G= XP_005265876.1:n.950-14092G=
XM_006714821.2:c.949+23167G= XP_006714884.1:n.949+23167G=
XM_011534435.1:c.1057+15425G= XP_011532737.1:n.1057+15425G=
XM_011534436.1:c.1058-14079G= XP_011532738.1:n.1058-14079G=
XM_011534437.1:c.1058-6669G= XP_011532739.1:n.1058-6669G=
XM_011534439.1:c.1058-14092G= XP_011532741.1:n.1058-14092G=
XM_005265818.3:c.950-6669G= XP_005265875.1:n.950-6669G=
XM_006714821.3:c.949+23167G= XP_006714884.1:n.949+23167G=
XM_011534437.2:c.1058-6669G= XP_011532739.1:n.1058-6669G=
XR_001742950.1:n.597C=
NM_000679.4:c.949+23167G= MANE Select NP_000670.1:n.949+23167G=