Canonical Allele Identifier: CA3498356
Gene: ADRB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 703863
ClinVar RCV Id: RCV000873645
dbSNP Id: rs33957121
ExAC: 5:148206460 C / T
gnomAD v2: 5-148206460-C-T
gnomAD v3: 5-148826897-C-T
gnomAD v4: 5-148826897-C-T
MyVariant Identifiers: chr5:g.148206460C>T (hg19) chr5:g.148826897C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148826897C>T , CM000667.2:g.148826897C>T GRCh38
NC_000005.9:g.148206460C>T , CM000667.1:g.148206460C>T GRCh37
NC_000005.8:g.148186653C>T NCBI36
NG_016421.1:g.5305C>T
NG_016421.2:g.5305C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.66C>T MANE Select ENSP00000305372.4:p.His22=
ENST00000305988.5:c.66C>T ENSP00000305372.4:p.His22=
NM_000024.5:c.66C>T NP_000015.1:p.His22=
NM_000024.6:c.66C>T MANE Select NP_000015.2:p.His22=
Search 100 bp 5'
Search 100 bp 3'