Canonical Allele Identifier: CA806475325

Gene: ADRA1B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159940107C>G , CM000667.2:g.159940107C>G	GRCh38
NC_000005.9:g.159367114C>G , CM000667.1:g.159367114C>G	GRCh37
NC_000005.8:g.159299692C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+22253C>G MANE Select	ENSP00000306662.3:n.949+22253C>G
ENST00000306675.3:c.949+22253C>G	ENSP00000306662.3:n.949+22253C>G
NM_000679.3:c.949+22253C>G	NP_000670.1:n.949+22253C>G
XM_005265818.2:c.950-7583C>G	XP_005265875.1:n.950-7583C>G
XM_005265819.2:c.950-15006C>G	XP_005265876.1:n.950-15006C>G
XM_006714821.2:c.949+22253C>G	XP_006714884.1:n.949+22253C>G
XM_011534435.1:c.1057+14511C>G	XP_011532737.1:n.1057+14511C>G
XM_011534436.1:c.1057+14511C>G	XP_011532738.1:n.1057+14511C>G
XM_011534437.1:c.1058-7583C>G	XP_011532739.1:n.1058-7583C>G
XM_011534439.1:c.1057+14511C>G	XP_011532741.1:n.1057+14511C>G
XM_005265818.3:c.950-7583C>G	XP_005265875.1:n.950-7583C>G
XM_006714821.3:c.949+22253C>G	XP_006714884.1:n.949+22253C>G
XM_011534437.2:c.1058-7583C>G	XP_011532739.1:n.1058-7583C>G
XR_001742950.1:n.1511G>C
NM_000679.4:c.949+22253C>G MANE Select	NP_000670.1:n.949+22253C>G