Canonical Allele Identifier: CA127363
Gene: ADRB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17744
ClinVar RCV Id: RCV000019320
dbSNP Id: rs1800888

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827322C>T , CM000667.2:g.148827322C>T GRCh38
NC_000005.9:g.148206885C>T , CM000667.1:g.148206885C>T GRCh37
NC_000005.8:g.148187078C>T NCBI36
NG_016421.1:g.5730C>T
NG_016421.2:g.5730C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000305988.6:c.491C>T MANE Select ENSP00000305372.4:p.Thr164Ile
ENST00000305988.5:c.491C>T ENSP00000305372.4:p.Thr164Ile
NM_000024.5:c.491C>T NP_000015.1:p.Thr164Ile
NM_000024.6:c.491C>T MANE Select NP_000015.2:p.Thr164Ile