Canonical Allele Identifier: CA564102408

Gene: ADRA1B

Linked Data

• dbSNP Id: rs1182413551
• gnomAD v2: 5-159367929-T-A
• gnomAD v3: 5-159940922-T-A
• gnomAD v4: 5-159940922-T-A
• MyVariant Identifiers: chr5:g.159367929T>A (hg19) ; chr5:g.159940922T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159940922T>A , CM000667.2:g.159940922T>A	GRCh38
NC_000005.9:g.159367929T>A , CM000667.1:g.159367929T>A	GRCh37
NC_000005.8:g.159300507T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306675.5:c.949+23068T>A MANE Select	ENSP00000306662.3:n.949+23068T>A
ENST00000306675.3:c.949+23068T>A	ENSP00000306662.3:n.949+23068T>A
NM_000679.3:c.949+23068T>A	NP_000670.1:n.949+23068T>A
XM_005265818.2:c.950-6768T>A	XP_005265875.1:n.950-6768T>A
XM_005265819.2:c.950-14191T>A	XP_005265876.1:n.950-14191T>A
XM_006714821.2:c.949+23068T>A	XP_006714884.1:n.949+23068T>A
XM_011534435.1:c.1057+15326T>A	XP_011532737.1:n.1057+15326T>A
XM_011534436.1:c.1058-14178T>A	XP_011532738.1:n.1058-14178T>A
XM_011534437.1:c.1058-6768T>A	XP_011532739.1:n.1058-6768T>A
XM_011534439.1:c.1058-14191T>A	XP_011532741.1:n.1058-14191T>A
XM_005265818.3:c.950-6768T>A	XP_005265875.1:n.950-6768T>A
XM_006714821.3:c.949+23068T>A	XP_006714884.1:n.949+23068T>A
XM_011534437.2:c.1058-6768T>A	XP_011532739.1:n.1058-6768T>A
XR_001742950.1:n.696A>T
NM_000679.4:c.949+23068T>A MANE Select	NP_000670.1:n.949+23068T>A