Canonical Allele Identifier: CA130822943

Gene: ADRA1B

Linked Data

• dbSNP Id: rs75946789
• gnomAD v2: 5-159368009-T-C
• gnomAD v3: 5-159941002-T-C
• gnomAD v4: 5-159941002-T-C
• MyVariant Identifiers: chr5:g.159368009T>C (hg19) ; chr5:g.159941002T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159941002T>C , CM000667.2:g.159941002T>C	GRCh38
NC_000005.9:g.159368009T>C , CM000667.1:g.159368009T>C	GRCh37
NC_000005.8:g.159300587T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306675.5:c.949+23148T>C MANE Select	ENSP00000306662.3:n.949+23148T>C
ENST00000306675.3:c.949+23148T>C	ENSP00000306662.3:n.949+23148T>C
NM_000679.3:c.949+23148T>C	NP_000670.1:n.949+23148T>C
XM_005265818.2:c.950-6688T>C	XP_005265875.1:n.950-6688T>C
XM_005265819.2:c.950-14111T>C	XP_005265876.1:n.950-14111T>C
XM_006714821.2:c.949+23148T>C	XP_006714884.1:n.949+23148T>C
XM_011534435.1:c.1057+15406T>C	XP_011532737.1:n.1057+15406T>C
XM_011534436.1:c.1058-14098T>C	XP_011532738.1:n.1058-14098T>C
XM_011534437.1:c.1058-6688T>C	XP_011532739.1:n.1058-6688T>C
XM_011534439.1:c.1058-14111T>C	XP_011532741.1:n.1058-14111T>C
XM_005265818.3:c.950-6688T>C	XP_005265875.1:n.950-6688T>C
XM_006714821.3:c.949+23148T>C	XP_006714884.1:n.949+23148T>C
XM_011534437.2:c.1058-6688T>C	XP_011532739.1:n.1058-6688T>C
XR_001742950.1:n.616A>G
NM_000679.4:c.949+23148T>C MANE Select	NP_000670.1:n.949+23148T>C