Canonical Allele Identifier: CA447425503
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1240636601
MyVariant Identifiers: chr5:g.148206802T>A (hg19) chr5:g.148827239T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827239T>A , CM000667.2:g.148827239T>A GRCh38
NC_000005.9:g.148206802T>A , CM000667.1:g.148206802T>A GRCh37
NC_000005.8:g.148186995T>A NCBI36
NG_016421.1:g.5647T>A
NG_016421.2:g.5647T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000305988.6:c.408T>A MANE Select ENSP00000305372.4:p.Thr136=
ENST00000305988.5:c.408T>A ENSP00000305372.4:p.Thr136=
NM_000024.5:c.408T>A NP_000015.1:p.Thr136=
NM_000024.6:c.408T>A MANE Select NP_000015.2:p.Thr136=
Search 100 bp 5'
Search 100 bp 3'