Canonical Allele Identifier: CA52382139

Gene: ADRA2B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96115250_96115258dup , CM000664.2:g.96115250_96115258dup	GRCh38
NG_032950.1:g.5903_5911dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620793.2:c.903_911dup MANE Select	ENSP00000480573.1:p.Glu304_Glu305insGluGluGlu
ENST00000620793.1:c.903_911dup	ENSP00000480573.1:p.Glu304_Glu305insGluGluGlu
NM_000682.6:c.903_911dup	NP_000673.2:p.Glu304_Glu305insGluGluGlu
NM_000682.7:c.903_911dup MANE Select	NP_000673.2:p.Glu304_Glu305insGluGluGlu