Canonical Allele Identifier: CA214476020
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs779687399
MyVariant Identifiers: chr10:g.115804979A>C (hg19) chr10:g.114045220A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114045220A>C , CM000672.2:g.114045220A>C GRCh38
NC_000010.10:g.115804979A>C , CM000672.1:g.115804979A>C GRCh37
NC_000010.9:g.115794969A>C NCBI36
NG_012187.1:g.6174A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.1088A>C MANE Select ENSP00000358301.2:p.Asn363Thr
ENST00000369295.3:c.1088A>C ENSP00000358301.2:p.Asn363Thr
NM_000684.2:c.1088A>C NP_000675.1:p.Asn363Thr
NM_000684.3:c.1088A>C MANE Select NP_000675.1:p.Asn363Thr
Search 100 bp 5'
Search 100 bp 3'