Canonical Allele Identifier: CA361894568
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs2127359865
MyVariant Identifiers: chr5:g.148206817C>A (hg19) chr5:g.148827254C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827254C>A , CM000667.2:g.148827254C>A GRCh38
NC_000005.9:g.148206817C>A , CM000667.1:g.148206817C>A GRCh37
NC_000005.8:g.148187010C>A NCBI36
NG_016421.1:g.5662C>A
NG_016421.2:g.5662C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.423C>A MANE Select ENSP00000305372.4:p.Tyr141Ter
ENST00000305988.5:c.423C>A ENSP00000305372.4:p.Tyr141Ter
NM_000024.5:c.423C>A NP_000015.1:p.Tyr141Ter
NM_000024.6:c.423C>A MANE Select NP_000015.2:p.Tyr141Ter
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