Canonical Allele Identifier: CA11987000
Gene: ADRA1B HGNC NCBI

Linked Data

dbSNP Id: rs6892282

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159933478G>T , CM000667.2:g.159933478G>T GRCh38
NC_000005.9:g.159360485G>T , CM000667.1:g.159360485G>T GRCh37
NC_000005.8:g.159293063G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306675.5:c.949+15624G>T MANE Select ENSP00000306662.3:p.=
ENST00000306675.3:c.949+15624G>T ENSP00000306662.3:p.=
NM_000679.3:c.949+15624G>T NP_000670.1:p.=
XM_005265818.2:c.950-14212G>T XP_005265875.1:p.=
XM_005265819.2:c.949+15624G>T XP_005265876.1:p.=
XM_006714821.2:c.949+15624G>T XP_006714884.1:p.=
XM_011534435.1:c.1057+7882G>T XP_011532737.1:p.=
XM_011534436.1:c.1057+7882G>T XP_011532738.1:p.=
XM_011534437.1:c.1057+7882G>T XP_011532739.1:p.=
XM_011534439.1:c.1057+7882G>T XP_011532741.1:p.=
XM_005265818.3:c.950-14212G>T XP_005265875.1:p.=
XM_006714821.3:c.949+15624G>T XP_006714884.1:p.=
XM_011534437.2:c.1057+7882G>T XP_011532739.1:p.=
NM_000679.4:c.949+15624G>T MANE Select NP_000670.1:p.=