Canonical Allele Identifier: CA4714432
Gene: ADRB3 HGNC NCBI

Linked Data

dbSNP Id: rs201912869
gnomAD v2: 8-37823747-C-T
gnomAD v3: 8-37966229-C-T
gnomAD v4: 8-37966229-C-T
COSMIC: COSM300841

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37966229C>T , CM000670.2:g.37966229C>T GRCh38
NC_000008.10:g.37823747C>T , CM000670.1:g.37823747C>T GRCh37
NC_000008.9:g.37942904C>T NCBI36
NG_011936.1:g.5438G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000345060.5:c.241G>A MANE Select ENSP00000343782.3:p.Ala81Thr
ENST00000520341.2:n.369G>A
ENST00000345060.4:c.241G>A ENSP00000343782.3:p.Ala81Thr
ENST00000614635.1:c.241G>A ENSP00000480325.1:p.Ala81Thr
NM_000025.2:c.241G>A NP_000016.1:p.Ala81Thr
NM_000025.3:c.241G>A MANE Select NP_000016.1:p.Ala81Thr