Canonical Allele Identifier: CA1083529730

Gene: ADRA1B

Linked Data

• dbSNP Id: rs1755082771
• gnomAD v3: 5-159940058-T-C
• gnomAD v4: 5-159940058-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159940058T>C , CM000667.2:g.159940058T>C	GRCh38
NC_000005.9:g.159367065T>C , CM000667.1:g.159367065T>C	GRCh37
NC_000005.8:g.159299643T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+22204T>C MANE Select	ENSP00000306662.3:n.949+22204T>C
ENST00000306675.3:c.949+22204T>C	ENSP00000306662.3:n.949+22204T>C
NM_000679.3:c.949+22204T>C	NP_000670.1:n.949+22204T>C
XM_005265818.2:c.950-7632T>C	XP_005265875.1:n.950-7632T>C
XM_005265819.2:c.950-15055T>C	XP_005265876.1:n.950-15055T>C
XM_006714821.2:c.949+22204T>C	XP_006714884.1:n.949+22204T>C
XM_011534435.1:c.1057+14462T>C	XP_011532737.1:n.1057+14462T>C
XM_011534436.1:c.1057+14462T>C	XP_011532738.1:n.1057+14462T>C
XM_011534437.1:c.1058-7632T>C	XP_011532739.1:n.1058-7632T>C
XM_011534439.1:c.1057+14462T>C	XP_011532741.1:n.1057+14462T>C
XM_005265818.3:c.950-7632T>C	XP_005265875.1:n.950-7632T>C
XM_006714821.3:c.949+22204T>C	XP_006714884.1:n.949+22204T>C
XM_011534437.2:c.1058-7632T>C	XP_011532739.1:n.1058-7632T>C
XR_001742950.1:n.1560A>G
NM_000679.4:c.949+22204T>C MANE Select	NP_000670.1:n.949+22204T>C