Canonical Allele Identifier: CA660122473
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1261820615
gnomAD v3: 10-114045430-A-ACGG
gnomAD v4: 10-114045430-A-ACGG
MyVariant Identifiers: chr10:g.115805189_115805190insCGG (hg19) chr10:g.114045430_114045431insCGG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114045432_114045433insGCG , CM000672.2:g.114045432_114045433insGCG GRCh38
NC_000010.10:g.115805191_115805192insGCG , CM000672.1:g.115805191_115805192insGCG GRCh37
NC_000010.9:g.115795181_115795182insGCG NCBI36
NG_012187.1:g.6386_6387insGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.1300_1301insGCG MANE Select ENSP00000358301.2:p.Asp433_Asp434insGly
ENST00000369295.3:c.1300_1301insGCG ENSP00000358301.2:p.Asp433_Asp434insGly
NM_000684.2:c.1300_1301insGCG NP_000675.1:p.Asp433_Asp434insGly
NM_000684.3:c.1300_1301insGCG MANE Select NP_000675.1:p.Asp433_Asp434insGly
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