Canonical Allele Identifier: CA660119721
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1370015437
gnomAD v4: 10-114044088-G-A
MyVariant Identifiers: chr10:g.115803847G>A (hg19) chr10:g.114044088G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114044088G>A , CM000672.2:g.114044088G>A GRCh38
NC_000010.10:g.115803847G>A , CM000672.1:g.115803847G>A GRCh37
NC_000010.9:g.115793837G>A NCBI36
NG_012187.1:g.5042G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369295.4:c.-45G>A MANE Select ENSP00000358301.2:n.-45G>A
ENST00000369295.3:c.-45G>A ENSP00000358301.2:n.-45G>A
NM_000684.2:c.-45G>A NP_000675.1:n.-45G>A
NM_000684.3:c.-45G>A MANE Select NP_000675.1:n.-45G>A
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