Canonical Allele Identifier: CA4714394

Gene: ADRB3

Linked Data

• ClinVar Variation Id: 3091062
• ClinVar RCV Id: RCV004385448
• dbSNP Id: rs201338035
• ExAC: 8:37823528 C / A
• gnomAD v2: 8-37823528-C-A
• gnomAD v3: 8-37966010-C-A
• gnomAD v4: 8-37966010-C-A
• MyVariant Identifiers: chr8:g.37823528C>A (hg19) ; chr8:g.37966010C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37966010C>A , CM000670.2:g.37966010C>A	GRCh38
NC_000008.10:g.37823528C>A , CM000670.1:g.37823528C>A	GRCh37
NC_000008.9:g.37942685C>A	NCBI36
NG_011936.1:g.5657G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345060.5:c.460G>T MANE Select	ENSP00000343782.3:p.Ala154Ser
ENST00000520341.2:n.588G>T
ENST00000345060.4:c.460G>T	ENSP00000343782.3:p.Ala154Ser
ENST00000614635.1:c.460G>T	ENSP00000480325.1:p.Ala154Ser
NM_000025.2:c.460G>T	NP_000016.1:p.Ala154Ser
NM_000025.3:c.460G>T MANE Select	NP_000016.1:p.Ala154Ser