Canonical Allele Identifier: CA471615612
Gene: ADRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.115803960C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114044201C>G , CM000672.2:g.114044201C>G GRCh38
NC_000010.10:g.115803960C>G , CM000672.1:g.115803960C>G GRCh37
NC_000010.9:g.115793950C>G NCBI36
NG_012187.1:g.5155C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369295.4:c.69C>G MANE Select ENSP00000358301.2:p.Pro23=
ENST00000369295.3:c.69C>G ENSP00000358301.2:p.Pro23=
NM_000684.2:c.69C>G NP_000675.1:p.Pro23=
NM_000684.3:c.69C>G MANE Select NP_000675.1:p.Pro23=