Canonical Allele Identifier: CA460494400
Gene: ADRB3 HGNC NCBI

Linked Data

gnomAD v4: 8-37966020-G-T
MyVariant Identifiers: chr8:g.37823538G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37966020G>T , CM000670.2:g.37966020G>T GRCh38
NC_000008.10:g.37823538G>T , CM000670.1:g.37823538G>T GRCh37
NC_000008.9:g.37942695G>T NCBI36
NG_011936.1:g.5647C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000345060.5:c.450C>A MANE Select ENSP00000343782.3:p.Thr150=
ENST00000520341.2:n.578C>A
ENST00000345060.4:c.450C>A ENSP00000343782.3:p.Thr150=
ENST00000614635.1:c.450C>A ENSP00000480325.1:p.Thr150=
NM_000025.2:c.450C>A NP_000016.1:p.Thr150=
NM_000025.3:c.450C>A MANE Select NP_000016.1:p.Thr150=