Canonical Allele Identifier: CA5698402
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs767449975
ExAC: 10:115804989 C / A
gnomAD v2: 10-115804989-C-A
gnomAD v4: 10-114045230-C-A
MyVariant Identifiers: chr10:g.115804989C>A (hg19) chr10:g.114045230C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114045230C>A , CM000672.2:g.114045230C>A GRCh38
NC_000010.10:g.115804989C>A , CM000672.1:g.115804989C>A GRCh37
NC_000010.9:g.115794979C>A NCBI36
NG_012187.1:g.6184C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.1098C>A MANE Select ENSP00000358301.2:p.Gly366=
ENST00000369295.3:c.1098C>A ENSP00000358301.2:p.Gly366=
NM_000684.2:c.1098C>A NP_000675.1:p.Gly366=
NM_000684.3:c.1098C>A MANE Select NP_000675.1:p.Gly366=
Search 100 bp 5'
Search 100 bp 3'