Canonical Allele Identifier: CA130817047

Gene: ADRA1B

Linked Data

• dbSNP Id: rs934916366
• MyVariant Identifiers: chr5:g.159360524G>T (hg19) ; chr5:g.159933517G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159933517G>T , CM000667.2:g.159933517G>T	GRCh38
NC_000005.9:g.159360524G>T , CM000667.1:g.159360524G>T	GRCh37
NC_000005.8:g.159293102G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306675.5:c.949+15663G>T MANE Select	ENSP00000306662.3:n.949+15663G>T
ENST00000306675.3:c.949+15663G>T	ENSP00000306662.3:n.949+15663G>T
NM_000679.3:c.949+15663G>T	NP_000670.1:n.949+15663G>T
XM_005265818.2:c.950-14173G>T	XP_005265875.1:n.950-14173G>T
XM_005265819.2:c.949+15663G>T	XP_005265876.1:n.949+15663G>T
XM_006714821.2:c.949+15663G>T	XP_006714884.1:n.949+15663G>T
XM_011534435.1:c.1057+7921G>T	XP_011532737.1:n.1057+7921G>T
XM_011534436.1:c.1057+7921G>T	XP_011532738.1:n.1057+7921G>T
XM_011534437.1:c.1057+7921G>T	XP_011532739.1:n.1057+7921G>T
XM_011534439.1:c.1057+7921G>T	XP_011532741.1:n.1057+7921G>T
XM_005265818.3:c.950-14173G>T	XP_005265875.1:n.950-14173G>T
XM_006714821.3:c.949+15663G>T	XP_006714884.1:n.949+15663G>T
XM_011534437.2:c.1057+7921G>T	XP_011532739.1:n.1057+7921G>T
NM_000679.4:c.949+15663G>T MANE Select	NP_000670.1:n.949+15663G>T