Canonical Allele Identifier: CA5698442
Gene: ADRB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3044684
ClinVar RCV Id: RCV003941858
dbSNP Id: rs545652970
ExAC: 10:115805130 C / G
gnomAD v2: 10-115805130-C-G
gnomAD v3: 10-114045371-C-G
gnomAD v4: 10-114045371-C-G
MyVariant Identifiers: chr10:g.115805130C>G (hg19) chr10:g.114045371C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114045371C>G , CM000672.2:g.114045371C>G GRCh38
NC_000010.10:g.115805130C>G , CM000672.1:g.115805130C>G GRCh37
NC_000010.9:g.115795120C>G NCBI36
NG_012187.1:g.6325C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.1239C>G MANE Select ENSP00000358301.2:p.Gly413=
ENST00000369295.3:c.1239C>G ENSP00000358301.2:p.Gly413=
NM_000684.2:c.1239C>G NP_000675.1:p.Gly413=
NM_000684.3:c.1239C>G MANE Select NP_000675.1:p.Gly413=
Search 100 bp 5'
Search 100 bp 3'