Canonical Allele Identifier: CA3498500
Gene: ADRB2 HGNC NCBI
COSMIC:
COSM3812433 (not active)
MyVariant.info:
GRCh38 chr5:g.148827884G>C
GRCh37 chr5:g.148207447G>C
gnomAD v2:
5:148207447 G / C
gnomAD v3:
5:148827884 G / C
gnomAD v4:
chr5-148827884-G-C
Joint Max Group AF 0.47357358 (EAS)
Genomes Max Group AF 0.43690826 (EAS)
Exomes Max Group AF 0.47669641 (EAS)
ClinVar RCV:
RCV001639295
ClinVar Variation:
1236780
dbSNP:
1042719
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827884G>C , CM000667.2:g.148827884G>C GRCh38
NC_000005.9:g.148207447G>C , CM000667.1:g.148207447G>C GRCh37
NC_000005.8:g.148187640G>C NCBI36
NG_016421.1:g.6292G>C
NG_016421.2:g.6292G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.1053G>C MANE Select ENSP00000305372.4:p.Gly351=
ENST00000305988.5:c.1053G>C ENSP00000305372.4:p.Gly351=
NM_000024.5:c.1053G>C NP_000015.1:p.Gly351=
NM_000024.6:c.1053G>C MANE Select NP_000015.2:p.Gly351=
Search 100 bp 5'
Search 100 bp 3'