Canonical Allele Identifier: CA12066412
Gene: ADRB2 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.148826465C>T
GRCh37 chr5:g.148206028C>T
gnomAD v2:
5:148206028 C / T
gnomAD v3:
5:148826465 C / T
gnomAD v4:
chr5-148826465-C-T
Joint Max Group AF 0.89986225 (EAS)
Genomes Max Group AF 0.88718286 (EAS)
Exomes Max Group AF 0.89884465 (EAS)
ClinVar RCV:
RCV001673954
ClinVar Variation:
1259578
dbSNP:
11959427
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148826465C>T , CM000667.2:g.148826465C>T GRCh38
NC_000005.9:g.148206028C>T , CM000667.1:g.148206028C>T GRCh37
NC_000005.8:g.148186221C>T NCBI36
NG_016421.1:g.4873C>T
NG_016421.2:g.4873C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.5:c.-367C>T ENSP00000305372.4:n.-367C>T
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