Canonical Allele Identifier: CA4714368
Gene: ADRB3 HGNC NCBI

Linked Data

dbSNP Id: rs753105162
ExAC: 8:37823322 G / C
gnomAD v2: 8-37823322-G-C
gnomAD v4: 8-37965804-G-C
MyVariant Identifiers: chr8:g.37823322G>C (hg19) chr8:g.37965804G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37965804G>C , CM000670.2:g.37965804G>C GRCh38
NC_000008.10:g.37823322G>C , CM000670.1:g.37823322G>C GRCh37
NC_000008.9:g.37942479G>C NCBI36
NG_011936.1:g.5863C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000345060.5:c.666C>G MANE Select ENSP00000343782.3:p.Phe222Leu
ENST00000520341.2:n.794C>G
ENST00000647937.1:c.150C>G ENSP00000497740.1:p.Phe50Leu
ENST00000345060.4:c.666C>G ENSP00000343782.3:p.Phe222Leu
ENST00000614635.1:c.666C>G ENSP00000480325.1:p.Phe222Leu
NM_000025.2:c.666C>G NP_000016.1:p.Phe222Leu
NM_000025.3:c.666C>G MANE Select NP_000016.1:p.Phe222Leu
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