Canonical Allele Identifier: CA175071897
Gene: ADRB3 HGNC NCBI

Linked Data

dbSNP Id: rs976013636
gnomAD v2: 8-37823522-T-C
gnomAD v3: 8-37966004-T-C
gnomAD v4: 8-37966004-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37966004T>C , CM000670.2:g.37966004T>C GRCh38
NC_000008.10:g.37823522T>C , CM000670.1:g.37823522T>C GRCh37
NC_000008.9:g.37942679T>C NCBI36
NG_011936.1:g.5663A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000345060.5:c.466A>G MANE Select ENSP00000343782.3:p.Thr156Ala
ENST00000520341.2:n.594A>G
ENST00000345060.4:c.466A>G ENSP00000343782.3:p.Thr156Ala
ENST00000614635.1:c.466A>G ENSP00000480325.1:p.Thr156Ala
NM_000025.2:c.466A>G NP_000016.1:p.Thr156Ala
NM_000025.3:c.466A>G MANE Select NP_000016.1:p.Thr156Ala