Canonical Allele Identifier: CA447425601
Gene: ADRB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.148206886C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827323C>T , CM000667.2:g.148827323C>T GRCh38
NC_000005.9:g.148206886C>T , CM000667.1:g.148206886C>T GRCh37
NC_000005.8:g.148187079C>T NCBI36
NG_016421.1:g.5731C>T
NG_016421.2:g.5731C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.492C>T MANE Select ENSP00000305372.4:p.Thr164=
ENST00000305988.5:c.492C>T ENSP00000305372.4:p.Thr164=
NM_000024.5:c.492C>T NP_000015.1:p.Thr164=
NM_000024.6:c.492C>T MANE Select NP_000015.2:p.Thr164=