Canonical Allele Identifier: CA447425546
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs2127359876
MyVariant Identifiers: chr5:g.148206871T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827308T>C , CM000667.2:g.148827308T>C GRCh38
NC_000005.9:g.148206871T>C , CM000667.1:g.148206871T>C GRCh37
NC_000005.8:g.148187064T>C NCBI36
NG_016421.1:g.5716T>C
NG_016421.2:g.5716T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.477T>C MANE Select ENSP00000305372.4:p.Ile159=
ENST00000305988.5:c.477T>C ENSP00000305372.4:p.Ile159=
NM_000024.5:c.477T>C NP_000015.1:p.Ile159=
NM_000024.6:c.477T>C MANE Select NP_000015.2:p.Ile159=