Canonical Allele Identifier: CA660119642
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1467413413
gnomAD v3: 10-114043930-G-A
gnomAD v4: 10-114043930-G-A
MyVariant Identifiers: chr10:g.115803689G>A (hg19) chr10:g.114043930G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114043930G>A , CM000672.2:g.114043930G>A GRCh38
NC_000010.10:g.115803689G>A , CM000672.1:g.115803689G>A GRCh37
NC_000010.9:g.115793679G>A NCBI36
NG_012187.1:g.4884G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.-203G>A MANE Select ENSP00000358301.2:n.-203G>A
NM_000684.3:c.-203G>A MANE Select NP_000675.1:n.-203G>A
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