Canonical Allele Identifier: CA447425798
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1359011932
gnomAD v2: 5-148207264-C-T
gnomAD v4: 5-148827701-C-T
MyVariant Identifiers: chr5:g.148207264C>T (hg19) chr5:g.148827701C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827701C>T , CM000667.2:g.148827701C>T GRCh38
NC_000005.9:g.148207264C>T , CM000667.1:g.148207264C>T GRCh37
NC_000005.8:g.148187457C>T NCBI36
NG_016421.1:g.6109C>T
NG_016421.2:g.6109C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.870C>T MANE Select ENSP00000305372.4:p.Phe290=
ENST00000305988.5:c.870C>T ENSP00000305372.4:p.Phe290=
NM_000024.5:c.870C>T NP_000015.1:p.Phe290=
NM_000024.6:c.870C>T MANE Select NP_000015.2:p.Phe290=
Search 100 bp 5'
Search 100 bp 3'