Canonical Allele Identifier: CA4714389
Gene: ADRB3 HGNC NCBI

Linked Data

dbSNP Id: rs764367690
gnomAD v2: 8-37823483-A-G
gnomAD v3: 8-37965965-A-G
gnomAD v4: 8-37965965-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37965965A>G , CM000670.2:g.37965965A>G GRCh38
NC_000008.10:g.37823483A>G , CM000670.1:g.37823483A>G GRCh37
NC_000008.9:g.37942640A>G NCBI36
NG_011936.1:g.5702T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000345060.5:c.505T>C MANE Select ENSP00000343782.3:p.Ser169Pro
ENST00000520341.2:n.633T>C
ENST00000345060.4:c.505T>C ENSP00000343782.3:p.Ser169Pro
ENST00000614635.1:c.505T>C ENSP00000480325.1:p.Ser169Pro
NM_000025.2:c.505T>C NP_000016.1:p.Ser169Pro
NM_000025.3:c.505T>C MANE Select NP_000016.1:p.Ser169Pro