Canonical Allele Identifier: CA5698308
Gene: ADRB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 782120
ClinVar RCV Id: RCV000963467
dbSNP Id: rs61729407
ExAC: 10:115804431 C / T
gnomAD v2: 10-115804431-C-T
gnomAD v3: 10-114044672-C-T
gnomAD v4: 10-114044672-C-T
MyVariant Identifiers: chr10:g.115804431C>T (hg19) chr10:g.114044672C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114044672C>T , CM000672.2:g.114044672C>T GRCh38
NC_000010.10:g.115804431C>T , CM000672.1:g.115804431C>T GRCh37
NC_000010.9:g.115794421C>T NCBI36
NG_012187.1:g.5626C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.540C>T MANE Select ENSP00000358301.2:p.Cys180=
ENST00000369295.3:c.540C>T ENSP00000358301.2:p.Cys180=
NM_000684.2:c.540C>T NP_000675.1:p.Cys180=
NM_000684.3:c.540C>T MANE Select NP_000675.1:p.Cys180=
Search 100 bp 5'
Search 100 bp 3'