Canonical Allele Identifier: CA5698445
Gene: ADRB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 778968
ClinVar RCV Id: RCV000959707
dbSNP Id: rs542444851
ExAC: 10:115805208 G / A
gnomAD v2: 10-115805208-G-A
gnomAD v3: 10-114045449-G-A
gnomAD v4: 10-114045449-G-A
MyVariant Identifiers: chr10:g.115805208G>A (hg19) chr10:g.114045449G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114045449G>A , CM000672.2:g.114045449G>A GRCh38
NC_000010.10:g.115805208G>A , CM000672.1:g.115805208G>A GRCh37
NC_000010.9:g.115795198G>A NCBI36
NG_012187.1:g.6403G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.1317G>A MANE Select ENSP00000358301.2:p.Thr439=
ENST00000369295.3:c.1317G>A ENSP00000358301.2:p.Thr439=
NM_000684.2:c.1317G>A NP_000675.1:p.Thr439=
NM_000684.3:c.1317G>A MANE Select NP_000675.1:p.Thr439=
Search 100 bp 5'
Search 100 bp 3'