Canonical Allele Identifier: CA596113246
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs754880345
gnomAD v2: 10-115805175-G-GGAC
gnomAD v3: 10-114045416-G-GGAC
gnomAD v4: 10-114045416-G-GGAC
MyVariant Identifiers: chr10:g.115805181_115805182insGAC (hg19) chr10:g.115805178_115805179insGAC (hg19) chr10:g.115805175_115805176insGAC (hg19) chr10:g.114045422_114045423insGAC (hg38) chr10:g.114045416_114045417insGAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114045431_114045433dup , CM000672.2:g.114045431_114045433dup GRCh38
NC_000010.10:g.115805190_115805192dup , CM000672.1:g.115805190_115805192dup GRCh37
NC_000010.9:g.115795180_115795182dup NCBI36
NG_012187.1:g.6385_6387dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.1299_1301dup MANE Select ENSP00000358301.2:p.Asp434_Val435insAsp
ENST00000369295.3:c.1299_1301dup ENSP00000358301.2:p.Asp434_Val435insAsp
NM_000684.2:c.1299_1301dup NP_000675.1:p.Asp434_Val435insAsp
NM_000684.3:c.1299_1301dup MANE Select NP_000675.1:p.Asp434_Val435insAsp
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