Canonical Allele Identifier: CA660119684
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1350610518
gnomAD v3: 10-114044001-G-C
gnomAD v4: 10-114044001-G-C
MyVariant Identifiers: chr10:g.115803760G>C (hg19) chr10:g.114044001G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114044001G>C , CM000672.2:g.114044001G>C GRCh38
NC_000010.10:g.115803760G>C , CM000672.1:g.115803760G>C GRCh37
NC_000010.9:g.115793750G>C NCBI36
NG_012187.1:g.4955G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.-132G>C MANE Select ENSP00000358301.2:n.-132G>C
NM_000684.3:c.-132G>C MANE Select NP_000675.1:n.-132G>C
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