Canonical Allele Identifier: CA806475777

Gene: ADRA1B

Linked Data

• dbSNP Id: rs1442930337
• MyVariant Identifiers: chr5:g.159368067T>C (hg19) ; chr5:g.159941060T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159941060T>C , CM000667.2:g.159941060T>C	GRCh38
NC_000005.9:g.159368067T>C , CM000667.1:g.159368067T>C	GRCh37
NC_000005.8:g.159300645T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306675.5:c.949+23206T>C MANE Select	ENSP00000306662.3:n.949+23206T>C
ENST00000306675.3:c.949+23206T>C	ENSP00000306662.3:n.949+23206T>C
NM_000679.3:c.949+23206T>C	NP_000670.1:n.949+23206T>C
XM_005265818.2:c.950-6630T>C	XP_005265875.1:n.950-6630T>C
XM_005265819.2:c.950-14053T>C	XP_005265876.1:n.950-14053T>C
XM_006714821.2:c.949+23206T>C	XP_006714884.1:n.949+23206T>C
XM_011534435.1:c.1057+15464T>C	XP_011532737.1:n.1057+15464T>C
XM_011534436.1:c.1058-14040T>C	XP_011532738.1:n.1058-14040T>C
XM_011534437.1:c.1058-6630T>C	XP_011532739.1:n.1058-6630T>C
XM_011534439.1:c.1058-14053T>C	XP_011532741.1:n.1058-14053T>C
XM_005265818.3:c.950-6630T>C	XP_005265875.1:n.950-6630T>C
XM_006714821.3:c.949+23206T>C	XP_006714884.1:n.949+23206T>C
XM_011534437.2:c.1058-6630T>C	XP_011532739.1:n.1058-6630T>C
XR_001742950.1:n.558A>G
NM_000679.4:c.949+23206T>C MANE Select	NP_000670.1:n.949+23206T>C