Canonical Allele Identifier: CA4714353
Gene: ADRB3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37965685G>C , CM000670.2:g.37965685G>C GRCh38
NC_000008.10:g.37823203G>C , CM000670.1:g.37823203G>C GRCh37
NC_000008.9:g.37942360G>C NCBI36
NG_011936.1:g.5982C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000345060.5:c.785C>G MANE Select ENSP00000343782.3:p.Pro262Arg
ENST00000520341.2:n.913C>G
ENST00000647937.1:c.269C>G ENSP00000497740.1:p.Pro90Arg
ENST00000345060.4:c.785C>G ENSP00000343782.3:p.Pro262Arg
ENST00000520341.1:n.60C>G
ENST00000614635.1:c.785C>G ENSP00000480325.1:p.Pro262Arg
NM_000025.2:c.785C>G NP_000016.1:p.Pro262Arg
NM_000025.3:c.785C>G MANE Select NP_000016.1:p.Pro262Arg