Canonical Allele Identifier: CA806475425

Gene: ADRA1B

Linked Data

• dbSNP Id: rs1355858642
• gnomAD v3: 5-159940312-C-T
• gnomAD v4: 5-159940312-C-T
• MyVariant Identifiers: chr5:g.159367319C>T (hg19) ; chr5:g.159940312C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159940312C>T , CM000667.2:g.159940312C>T	GRCh38
NC_000005.9:g.159367319C>T , CM000667.1:g.159367319C>T	GRCh37
NC_000005.8:g.159299897C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+22458C>T MANE Select	ENSP00000306662.3:n.949+22458C>T
ENST00000306675.3:c.949+22458C>T	ENSP00000306662.3:n.949+22458C>T
NM_000679.3:c.949+22458C>T	NP_000670.1:n.949+22458C>T
XM_005265818.2:c.950-7378C>T	XP_005265875.1:n.950-7378C>T
XM_005265819.2:c.950-14801C>T	XP_005265876.1:n.950-14801C>T
XM_006714821.2:c.949+22458C>T	XP_006714884.1:n.949+22458C>T
XM_011534435.1:c.1057+14716C>T	XP_011532737.1:n.1057+14716C>T
XM_011534436.1:c.1057+14716C>T	XP_011532738.1:n.1057+14716C>T
XM_011534437.1:c.1058-7378C>T	XP_011532739.1:n.1058-7378C>T
XM_011534439.1:c.1057+14716C>T	XP_011532741.1:n.1057+14716C>T
XM_005265818.3:c.950-7378C>T	XP_005265875.1:n.950-7378C>T
XM_006714821.3:c.949+22458C>T	XP_006714884.1:n.949+22458C>T
XM_011534437.2:c.1058-7378C>T	XP_011532739.1:n.1058-7378C>T
XR_001742950.1:n.1306G>A
NM_000679.4:c.949+22458C>T MANE Select	NP_000670.1:n.949+22458C>T