Canonical Allele Identifier: CA471616041
Gene: ADRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.115804464C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114044705C>T , CM000672.2:g.114044705C>T GRCh38
NC_000010.10:g.115804464C>T , CM000672.1:g.115804464C>T GRCh37
NC_000010.9:g.115794454C>T NCBI36
NG_012187.1:g.5659C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.573C>T MANE Select ENSP00000358301.2:p.Phe191=
ENST00000369295.3:c.573C>T ENSP00000358301.2:p.Phe191=
NM_000684.2:c.573C>T NP_000675.1:p.Phe191=
NM_000684.3:c.573C>T MANE Select NP_000675.1:p.Phe191=