Canonical Allele Identifier: CA660119713
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1469540954
gnomAD v3: 10-114044057-G-T
gnomAD v4: 10-114044057-G-T
MyVariant Identifiers: chr10:g.115803816G>T (hg19) chr10:g.114044057G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114044057G>T , CM000672.2:g.114044057G>T GRCh38
NC_000010.10:g.115803816G>T , CM000672.1:g.115803816G>T GRCh37
NC_000010.9:g.115793806G>T NCBI36
NG_012187.1:g.5011G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.-76G>T MANE Select ENSP00000358301.2:n.-76G>T
ENST00000369295.3:c.-76G>T ENSP00000358301.2:n.-76G>T
NM_000684.2:c.-76G>T NP_000675.1:n.-76G>T
NM_000684.3:c.-76G>T MANE Select NP_000675.1:n.-76G>T
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