Canonical Allele Identifier: CA3498459
Gene: ADRB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 784824
ClinVar RCV Id: RCV000966605 RCV003928414
dbSNP Id: rs536975083
ExAC: 5:148207165 A / T
gnomAD v2: 5-148207165-A-T
gnomAD v3: 5-148827602-A-T
gnomAD v4: 5-148827602-A-T
MyVariant Identifiers: chr5:g.148207165A>T (hg19) chr5:g.148827602A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827602A>T , CM000667.2:g.148827602A>T GRCh38
NC_000005.9:g.148207165A>T , CM000667.1:g.148207165A>T GRCh37
NC_000005.8:g.148187358A>T NCBI36
NG_016421.1:g.6010A>T
NG_016421.2:g.6010A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.771A>T MANE Select ENSP00000305372.4:p.Gly257=
ENST00000305988.5:c.771A>T ENSP00000305372.4:p.Gly257=
NM_000024.5:c.771A>T NP_000015.1:p.Gly257=
NM_000024.6:c.771A>T MANE Select NP_000015.2:p.Gly257=
Search 100 bp 5'
Search 100 bp 3'