Canonical Allele Identifier: CA471618570
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1847549079
gnomAD v4: 10-114045434-T-C
MyVariant Identifiers: chr10:g.115805193T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114045434T>C , CM000672.2:g.114045434T>C GRCh38
NC_000010.10:g.115805193T>C , CM000672.1:g.115805193T>C GRCh37
NC_000010.9:g.115795183T>C NCBI36
NG_012187.1:g.6388T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.1302T>C MANE Select ENSP00000358301.2:p.Asp434=
ENST00000369295.3:c.1302T>C ENSP00000358301.2:p.Asp434=
NM_000684.2:c.1302T>C NP_000675.1:p.Asp434=
NM_000684.3:c.1302T>C MANE Select NP_000675.1:p.Asp434=
Search 100 bp 5'
Search 100 bp 3'