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: CA370693537
Gene: ADRB3 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37965698G>T , CM000670.2:g.37965698G>T GRCh38
NC_000008.10:g.37823216G>T , CM000670.1:g.37823216G>T GRCh37
NC_000008.9:g.37942373G>T NCBI36
NG_011936.1:g.5969C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000345060.5:c.772C>A MANE Select ENSP00000343782.3:p.Leu258Met
ENST00000520341.2:n.900C>A
ENST00000647937.1:c.256C>A ENSP00000497740.1:p.Leu86Met
ENST00000345060.4:c.772C>A ENSP00000343782.3:p.Leu258Met
ENST00000520341.1:n.47C>A
ENST00000614635.1:c.772C>A ENSP00000480325.1:p.Leu258Met
NM_000025.2:c.772C>A NP_000016.1:p.Leu258Met
NM_000025.3:c.772C>A MANE Select NP_000016.1:p.Leu258Met