Canonical Allele Identifier: CA595778613
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1014758367
gnomAD v2: 10-115803680-A-AGCGGCGGCG
gnomAD v4: 10-114043921-A-AGCGGCGGCG
MyVariant Identifiers: chr10:g.115803692_115803693insGCGGCGGCG (hg19) chr10:g.115803680_115803681insGCGGCGGCG (hg19) chr10:g.114043933_114043934insGCGGCGGCG (hg38) chr10:g.114043921_114043922insGCGGCGGCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114043936_114043944dup , CM000672.2:g.114043936_114043944dup GRCh38
NC_000010.10:g.115803695_115803703dup , CM000672.1:g.115803695_115803703dup GRCh37
NC_000010.9:g.115793685_115793693dup NCBI36
NG_012187.1:g.4890_4898dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.-197_-189dup MANE Select ENSP00000358301.2:n.-197_-189dup
NM_000684.3:c.-197_-189dup MANE Select NP_000675.1:n.-197_-189dup
Search 100 bp 5'
Search 100 bp 3'