Canonical Allele Identifier: CA460494395
Gene: ADRB3 HGNC NCBI

Linked Data

dbSNP Id: rs1378075168
gnomAD v2: 8-37823535-C-T
gnomAD v3: 8-37966017-C-T
gnomAD v4: 8-37966017-C-T
MyVariant Identifiers: chr8:g.37823535C>T (hg19) chr8:g.37966017C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37966017C>T , CM000670.2:g.37966017C>T GRCh38
NC_000008.10:g.37823535C>T , CM000670.1:g.37823535C>T GRCh37
NC_000008.9:g.37942692C>T NCBI36
NG_011936.1:g.5650G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000345060.5:c.453G>A MANE Select ENSP00000343782.3:p.Lys151=
ENST00000520341.2:n.581G>A
ENST00000345060.4:c.453G>A ENSP00000343782.3:p.Lys151=
ENST00000614635.1:c.453G>A ENSP00000480325.1:p.Lys151=
NM_000025.2:c.453G>A NP_000016.1:p.Lys151=
NM_000025.3:c.453G>A MANE Select NP_000016.1:p.Lys151=
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