Canonical Allele Identifier: CA175071733
Gene: ADRB3 HGNC NCBI

Linked Data

dbSNP Id: rs200525008
gnomAD v3: 8-37965889-C-T
gnomAD v4: 8-37965889-C-T
MyVariant Identifiers: chr8:g.37823407C>T (hg19) chr8:g.37965889C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37965889C>T , CM000670.2:g.37965889C>T GRCh38
NC_000008.10:g.37823407C>T , CM000670.1:g.37823407C>T GRCh37
NC_000008.9:g.37942564C>T NCBI36
NG_011936.1:g.5778G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000345060.5:c.581G>A MANE Select ENSP00000343782.3:p.Arg194His
ENST00000520341.2:n.709G>A
ENST00000647937.1:c.65G>A ENSP00000497740.1:p.Arg22His
ENST00000345060.4:c.581G>A ENSP00000343782.3:p.Arg194His
ENST00000614635.1:c.581G>A ENSP00000480325.1:p.Arg194His
NM_000025.2:c.581G>A NP_000016.1:p.Arg194His
NM_000025.3:c.581G>A MANE Select NP_000016.1:p.Arg194His
Search 100 bp 5'
Search 100 bp 3'