Canonical Allele Identifier: CA361894213
Gene: ADRB2 HGNC NCBI

Linked Data

gnomAD v4: 5-148827096-T-G
MyVariant Identifiers: chr5:g.148206659T>G (hg19) chr5:g.148827096T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827096T>G , CM000667.2:g.148827096T>G GRCh38
NC_000005.9:g.148206659T>G , CM000667.1:g.148206659T>G GRCh37
NC_000005.8:g.148186852T>G NCBI36
NG_016421.1:g.5504T>G
NG_016421.2:g.5504T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000305988.6:c.265T>G MANE Select ENSP00000305372.4:p.Phe89Val
ENST00000305988.5:c.265T>G ENSP00000305372.4:p.Phe89Val
NM_000024.5:c.265T>G NP_000015.1:p.Phe89Val
NM_000024.6:c.265T>G MANE Select NP_000015.2:p.Phe89Val
Search 100 bp 5'
Search 100 bp 3'