Canonical Allele Identifier: CA130816847

Gene: ADRA1B

Linked Data

• dbSNP Id: rs781724852
• gnomAD v3: 5-159933349-A-G
• gnomAD v4: 5-159933349-A-G
• MyVariant Identifiers: chr5:g.159360356A>G (hg19) ; chr5:g.159933349A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159933349A>G , CM000667.2:g.159933349A>G	GRCh38
NC_000005.9:g.159360356A>G , CM000667.1:g.159360356A>G	GRCh37
NC_000005.8:g.159292934A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+15495A>G MANE Select	ENSP00000306662.3:n.949+15495A>G
ENST00000306675.3:c.949+15495A>G	ENSP00000306662.3:n.949+15495A>G
NM_000679.3:c.949+15495A>G	NP_000670.1:n.949+15495A>G
XM_005265818.2:c.950-14341A>G	XP_005265875.1:n.950-14341A>G
XM_005265819.2:c.949+15495A>G	XP_005265876.1:n.949+15495A>G
XM_006714821.2:c.949+15495A>G	XP_006714884.1:n.949+15495A>G
XM_011534435.1:c.1057+7753A>G	XP_011532737.1:n.1057+7753A>G
XM_011534436.1:c.1057+7753A>G	XP_011532738.1:n.1057+7753A>G
XM_011534437.1:c.1057+7753A>G	XP_011532739.1:n.1057+7753A>G
XM_011534439.1:c.1057+7753A>G	XP_011532741.1:n.1057+7753A>G
XM_005265818.3:c.950-14341A>G	XP_005265875.1:n.950-14341A>G
XM_006714821.3:c.949+15495A>G	XP_006714884.1:n.949+15495A>G
XM_011534437.2:c.1057+7753A>G	XP_011532739.1:n.1057+7753A>G
NM_000679.4:c.949+15495A>G MANE Select	NP_000670.1:n.949+15495A>G