Canonical Allele Identifier: CA660119646
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1554916080
gnomAD v3: 10-114043936-G-GGAGGCGGCA
gnomAD v4: 10-114043936-G-GGAGGCGGCA
MyVariant Identifiers: chr10:g.115803695_115803696insGAGGCGGCA (hg19) chr10:g.114043936_114043937insGAGGCGGCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114043937_114043938insAGGCGGCAG , CM000672.2:g.114043937_114043938insAGGCGGCAG GRCh38
NC_000010.10:g.115803696_115803697insAGGCGGCAG , CM000672.1:g.115803696_115803697insAGGCGGCAG GRCh37
NC_000010.9:g.115793686_115793687insAGGCGGCAG NCBI36
NG_012187.1:g.4891_4892insAGGCGGCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.-196_-195insAGGCGGCAG MANE Select ENSP00000358301.2:n.-196_-195insAGGCGGCAG
NM_000684.3:c.-196_-195insAGGCGGCAG MANE Select NP_000675.1:n.-196_-195insAGGCGGCAG
Search 100 bp 5'
Search 100 bp 3'