Canonical Allele Identifier: CA3498469
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs749002771
ExAC: 5:148207262 T / G
gnomAD v2: 5-148207262-T-G
gnomAD v3: 5-148827699-T-G
gnomAD v4: 5-148827699-T-G
MyVariant Identifiers: chr5:g.148207262T>G (hg19) chr5:g.148827699T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827699T>G , CM000667.2:g.148827699T>G GRCh38
NC_000005.9:g.148207262T>G , CM000667.1:g.148207262T>G GRCh37
NC_000005.8:g.148187455T>G NCBI36
NG_016421.1:g.6107T>G
NG_016421.2:g.6107T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.868T>G MANE Select ENSP00000305372.4:p.Phe290Val
ENST00000305988.5:c.868T>G ENSP00000305372.4:p.Phe290Val
NM_000024.5:c.868T>G NP_000015.1:p.Phe290Val
NM_000024.6:c.868T>G MANE Select NP_000015.2:p.Phe290Val
Search 100 bp 5'
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