Canonical Allele Identifier: CA11950140
Gene: ADRA1B HGNC NCBI

Linked Data

dbSNP Id: rs2030373

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159920474C>A , CM000667.2:g.159920474C>A GRCh38
NC_000005.9:g.159347481C>A , CM000667.1:g.159347481C>A GRCh37
NC_000005.8:g.159280059C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306675.5:c.949+2620C>A MANE Select ENSP00000306662.3:p.=
ENST00000306675.3:c.949+2620C>A ENSP00000306662.3:p.=
NM_000679.3:c.949+2620C>A NP_000670.1:p.=
XM_005265818.2:c.949+2620C>A XP_005265875.1:p.=
XM_005265819.2:c.949+2620C>A XP_005265876.1:p.=
XM_006714821.2:c.949+2620C>A XP_006714884.1:p.=
XM_011534435.1:c.949+2620C>A XP_011532737.1:p.=
XM_011534436.1:c.949+2620C>A XP_011532738.1:p.=
XM_011534437.1:c.949+2620C>A XP_011532739.1:p.=
XM_011534438.1:c.949+2620C>A XP_011532740.1:p.=
XM_011534439.1:c.949+2620C>A XP_011532741.1:p.=
XM_011534440.1:c.949+2620C>A XP_011532742.1:p.=
XM_005265818.3:c.949+2620C>A XP_005265875.1:p.=
XM_006714821.3:c.949+2620C>A XP_006714884.1:p.=
XM_011534437.2:c.949+2620C>A XP_011532739.1:p.=
XM_011534438.2:c.949+2620C>A XP_011532740.1:p.=
NM_000679.4:c.949+2620C>A MANE Select NP_000670.1:p.=