Canonical Allele Identifier: CA15415644
Gene: ADRA1B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10515807

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159937991G>A , CM000667.2:g.159937991G>A GRCh38
NC_000005.9:g.159364998G>A , CM000667.1:g.159364998G>A GRCh37
NC_000005.8:g.159297576G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_000679.3:c.949+20137G>A VV NP_000670.1:p.=
XM_005265818.2:c.950-9699G>A XP_005265875.1:p.=
XM_005265819.2:c.950-17122G>A XP_005265876.1:p.=
XM_006714821.2:c.949+20137G>A XP_006714884.1:p.=
XM_011534435.1:c.1057+12395G>A XP_011532737.1:p.=
XM_011534436.1:c.1057+12395G>A XP_011532738.1:p.=
XM_011534437.1:c.1058-9699G>A XP_011532739.1:p.=
XM_011534439.1:c.1057+12395G>A XP_011532741.1:p.=
XM_005265818.3:c.950-9699G>A XP_005265875.1:p.=
XM_006714821.3:c.949+20137G>A XP_006714884.1:p.=
XM_011534437.2:c.1058-9699G>A XP_011532739.1:p.=
XR_001742950.1:n.3627C>T
NM_000679.4:c.949+20137G>A VV MANE Preferred NP_000670.1:p.=
ENST00000306675.3:c.949+20137G>A ENSP00000306662.3:p.=