This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: CA370693456
Gene: ADRB3 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37965682A>G , CM000670.2:g.37965682A>G GRCh38
NC_000008.10:g.37823200A>G , CM000670.1:g.37823200A>G GRCh37
NC_000008.9:g.37942357A>G NCBI36
NG_011936.1:g.5985T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000345060.5:c.788T>C MANE Select ENSP00000343782.3:p.Val263Ala
ENST00000520341.2:n.916T>C
ENST00000647937.1:c.272T>C ENSP00000497740.1:p.Val91Ala
ENST00000345060.4:c.788T>C ENSP00000343782.3:p.Val263Ala
ENST00000520341.1:n.63T>C
ENST00000614635.1:c.788T>C ENSP00000480325.1:p.Val263Ala
NM_000025.2:c.788T>C NP_000016.1:p.Val263Ala
NM_000025.3:c.788T>C MANE Select NP_000016.1:p.Val263Ala