Canonical Allele Identifier: CA361894761
Gene: ADRB2 HGNC NCBI

Linked Data

gnomAD v4: 5-148827342-A-G
MyVariant Identifiers: chr5:g.148206905A>G (hg19) chr5:g.148827342A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827342A>G , CM000667.2:g.148827342A>G GRCh38
NC_000005.9:g.148206905A>G , CM000667.1:g.148206905A>G GRCh37
NC_000005.8:g.148187098A>G NCBI36
NG_016421.1:g.5750A>G
NG_016421.2:g.5750A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.511A>G MANE Select ENSP00000305372.4:p.Met171Val
ENST00000305988.5:c.511A>G ENSP00000305372.4:p.Met171Val
NM_000024.5:c.511A>G NP_000015.1:p.Met171Val
NM_000024.6:c.511A>G MANE Select NP_000015.2:p.Met171Val
Search 100 bp 5'
Search 100 bp 3'