Canonical Allele Identifier: CA5698228
Gene: ADRB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 717168
ClinVar RCV Id: RCV000889915
dbSNP Id: rs545019520
ExAC: 10:115803905 T / C
gnomAD v2: 10-115803905-T-C
gnomAD v3: 10-114044146-T-C
gnomAD v4: 10-114044146-T-C
MyVariant Identifiers: chr10:g.115803905T>C (hg19) chr10:g.114044146T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114044146T>C , CM000672.2:g.114044146T>C GRCh38
NC_000010.10:g.115803905T>C , CM000672.1:g.115803905T>C GRCh37
NC_000010.9:g.115793895T>C NCBI36
NG_012187.1:g.5100T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.14T>C MANE Select ENSP00000358301.2:p.Val5Ala
ENST00000369295.3:c.14T>C ENSP00000358301.2:p.Val5Ala
NM_000684.2:c.14T>C NP_000675.1:p.Val5Ala
NM_000684.3:c.14T>C MANE Select NP_000675.1:p.Val5Ala
Search 100 bp 5'
Search 100 bp 3'