Canonical Allele Identifier: CA5698414
Gene: ADRB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 735162
ClinVar RCV Id: RCV000910669
dbSNP Id: rs17875445
ExAC: 10:115805057 G / T
gnomAD v2: 10-115805057-G-T
gnomAD v3: 10-114045298-G-T
gnomAD v4: 10-114045298-G-T
MyVariant Identifiers: chr10:g.115805057G>T (hg19) chr10:g.114045298G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114045298G>T , CM000672.2:g.114045298G>T GRCh38
NC_000010.10:g.115805057G>T , CM000672.1:g.115805057G>T GRCh37
NC_000010.9:g.115795047G>T NCBI36
NG_012187.1:g.6252G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.1166G>T MANE Select ENSP00000358301.2:p.Gly389Val
ENST00000369295.3:c.1166G>T ENSP00000358301.2:p.Gly389Val
NM_000684.2:c.1166G>T NP_000675.1:p.Gly389Val
NM_000684.3:c.1166G>T MANE Select NP_000675.1:p.Gly389Val
Search 100 bp 5'
Search 100 bp 3'