Canonical Allele Identifier: CA1595317226
Gene: ADRA1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159940967A= , CM000667.2:g.159940967A= GRCh38
NC_000005.9:g.159367974A= , CM000667.1:g.159367974A= GRCh37
NC_000005.8:g.159300552A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306675.5:c.949+23113A= MANE Select ENSP00000306662.3:n.949+23113A=
ENST00000306675.3:c.949+23113A= ENSP00000306662.3:n.949+23113A=
NM_000679.3:c.949+23113A= NP_000670.1:n.949+23113A=
XM_005265818.2:c.950-6723A= XP_005265875.1:n.950-6723A=
XM_005265819.2:c.950-14146A= XP_005265876.1:n.950-14146A=
XM_006714821.2:c.949+23113A= XP_006714884.1:n.949+23113A=
XM_011534435.1:c.1057+15371A= XP_011532737.1:n.1057+15371A=
XM_011534436.1:c.1058-14133A= XP_011532738.1:n.1058-14133A=
XM_011534437.1:c.1058-6723A= XP_011532739.1:n.1058-6723A=
XM_011534439.1:c.1058-14146A= XP_011532741.1:n.1058-14146A=
XM_005265818.3:c.950-6723A= XP_005265875.1:n.950-6723A=
XM_006714821.3:c.949+23113A= XP_006714884.1:n.949+23113A=
XM_011534437.2:c.1058-6723A= XP_011532739.1:n.1058-6723A=
XR_001742950.1:n.651T=
NM_000679.4:c.949+23113A= MANE Select NP_000670.1:n.949+23113A=