Canonical Allele Identifier: CA806466404
Gene: ADRA1B HGNC NCBI

Linked Data

dbSNP Id: rs1479158845

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159924498G>A , CM000667.2:g.159924498G>A GRCh38
NC_000005.9:g.159351505G>A , CM000667.1:g.159351505G>A GRCh37
NC_000005.8:g.159284083G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306675.5:c.949+6644G>A MANE Select ENSP00000306662.3:n.949+6644G>A
ENST00000306675.3:c.949+6644G>A ENSP00000306662.3:n.949+6644G>A
NM_000679.3:c.949+6644G>A NP_000670.1:n.949+6644G>A
XM_005265818.2:c.949+6644G>A XP_005265875.1:n.949+6644G>A
XM_005265819.2:c.949+6644G>A XP_005265876.1:n.949+6644G>A
XM_006714821.2:c.949+6644G>A XP_006714884.1:n.949+6644G>A
XM_011534435.1:c.950-991G>A XP_011532737.1:n.950-991G>A
XM_011534436.1:c.950-991G>A XP_011532738.1:n.950-991G>A
XM_011534437.1:c.950-991G>A XP_011532739.1:n.950-991G>A
XM_011534438.1:c.950-991G>A XP_011532740.1:n.950-991G>A
XM_011534439.1:c.950-991G>A XP_011532741.1:n.950-991G>A
XM_011534440.1:c.950-991G>A XP_011532742.1:n.950-991G>A
XM_005265818.3:c.949+6644G>A XP_005265875.1:n.949+6644G>A
XM_006714821.3:c.949+6644G>A XP_006714884.1:n.949+6644G>A
XM_011534437.2:c.950-991G>A XP_011532739.1:n.950-991G>A
XM_011534438.2:c.950-991G>A XP_011532740.1:n.950-991G>A
NM_000679.4:c.949+6644G>A MANE Select NP_000670.1:n.949+6644G>A