Canonical Allele Identifier: CA370697628
Gene: ADRB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2253399
ClinVar RCV Id: RCV004110133
dbSNP Id: rs1808314734
gnomAD v3: 8-37966268-G-A
gnomAD v4: 8-37966268-G-A
MyVariant Identifiers: chr8:g.37823786G>A (hg19) chr8:g.37966268G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37966268G>A , CM000670.2:g.37966268G>A GRCh38
NC_000008.10:g.37823786G>A , CM000670.1:g.37823786G>A GRCh37
NC_000008.9:g.37942943G>A NCBI36
NG_011936.1:g.5399C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000345060.5:c.202C>T MANE Select ENSP00000343782.3:p.Leu68Phe
ENST00000520341.2:n.330C>T
ENST00000345060.4:c.202C>T ENSP00000343782.3:p.Leu68Phe
ENST00000614635.1:c.202C>T ENSP00000480325.1:p.Leu68Phe
NM_000025.2:c.202C>T NP_000016.1:p.Leu68Phe
NM_000025.3:c.202C>T MANE Select NP_000016.1:p.Leu68Phe
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