Canonical Allele Identifier: CA12074492
Gene: ADRA1B HGNC NCBI

Linked Data

dbSNP Id: rs13162302

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159940268A>G , CM000667.2:g.159940268A>G GRCh38
NC_000005.9:g.159367275A>G , CM000667.1:g.159367275A>G GRCh37
NC_000005.8:g.159299853A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306675.5:c.949+22414A>G MANE Select ENSP00000306662.3:p.=
ENST00000306675.3:c.949+22414A>G ENSP00000306662.3:p.=
NM_000679.3:c.949+22414A>G NP_000670.1:p.=
XM_005265818.2:c.950-7422A>G XP_005265875.1:p.=
XM_005265819.2:c.950-14845A>G XP_005265876.1:p.=
XM_006714821.2:c.949+22414A>G XP_006714884.1:p.=
XM_011534435.1:c.1057+14672A>G XP_011532737.1:p.=
XM_011534436.1:c.1057+14672A>G XP_011532738.1:p.=
XM_011534437.1:c.1058-7422A>G XP_011532739.1:p.=
XM_011534439.1:c.1057+14672A>G XP_011532741.1:p.=
XM_005265818.3:c.950-7422A>G XP_005265875.1:p.=
XM_006714821.3:c.949+22414A>G XP_006714884.1:p.=
XM_011534437.2:c.1058-7422A>G XP_011532739.1:p.=
XR_001742950.1:n.1350T>C
NM_000679.4:c.949+22414A>G MANE Select NP_000670.1:p.=