Canonical Allele Identifier: CA471618514
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs760326053
gnomAD v4: 10-114045362-C-T
MyVariant Identifiers: chr10:g.115805121C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114045362C>T , CM000672.2:g.114045362C>T GRCh38
NC_000010.10:g.115805121C>T , CM000672.1:g.115805121C>T GRCh37
NC_000010.9:g.115795111C>T NCBI36
NG_012187.1:g.6316C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.1230C>T MANE Select ENSP00000358301.2:p.Arg410=
ENST00000369295.3:c.1230C>T ENSP00000358301.2:p.Arg410=
NM_000684.2:c.1230C>T NP_000675.1:p.Arg410=
NM_000684.3:c.1230C>T MANE Select NP_000675.1:p.Arg410=
Search 100 bp 5'
Search 100 bp 3'