Canonical Allele Identifier: CA5698258
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs780643195
ExAC: 10:115804101 G / C
gnomAD v2: 10-115804101-G-C
gnomAD v3: 10-114044342-G-C
gnomAD v4: 10-114044342-G-C
MyVariant Identifiers: chr10:g.115804101G>C (hg19) chr10:g.114044342G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114044342G>C , CM000672.2:g.114044342G>C GRCh38
NC_000010.10:g.115804101G>C , CM000672.1:g.115804101G>C GRCh37
NC_000010.9:g.115794091G>C NCBI36
NG_012187.1:g.5296G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.210G>C MANE Select ENSP00000358301.2:p.Leu70=
ENST00000369295.3:c.210G>C ENSP00000358301.2:p.Leu70=
NM_000684.2:c.210G>C NP_000675.1:p.Leu70=
NM_000684.3:c.210G>C MANE Select NP_000675.1:p.Leu70=
Search 100 bp 5'
Search 100 bp 3'