Canonical Allele Identifier: CA11947255
Gene: ADRB2 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.148826178G>A
GRCh37 chr5:g.148205741G>A
gnomAD v2:
5:148205741 G / A
gnomAD v3:
5:148826178 G / A
gnomAD v4:
chr5-148826178-G-A
Joint Max Group AF 0.37871983 (AMR)
Genomes Max Group AF 0.37937207 (AMR)
Exomes Max Group AF 0.34212835 (NFE)
ClinVar RCV:
RCV001537123
ClinVar Variation:
1180015
dbSNP:
12654778
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148826178G>A , CM000667.2:g.148826178G>A GRCh38
NC_000005.9:g.148205741G>A , CM000667.1:g.148205741G>A GRCh37
NC_000005.8:g.148185934G>A NCBI36
NG_016421.1:g.4586G>A
NG_016421.2:g.4586G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.5:c.-654G>A ENSP00000305372.4:n.-654G>A
Search 100 bp 5'
Search 100 bp 3'