Canonical Allele Identifier: CA471615885
Gene: ADRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.115804453C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114044694C>T , CM000672.2:g.114044694C>T GRCh38
NC_000010.10:g.115804453C>T , CM000672.1:g.115804453C>T GRCh37
NC_000010.9:g.115794443C>T NCBI36
NG_012187.1:g.5648C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.562C>T MANE Select ENSP00000358301.2:p.Leu188=
ENST00000369295.3:c.562C>T ENSP00000358301.2:p.Leu188=
NM_000684.2:c.562C>T NP_000675.1:p.Leu188=
NM_000684.3:c.562C>T MANE Select NP_000675.1:p.Leu188=