Canonical Allele Identifier: CA361894728
Gene: ADRB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.148206891T>A (hg19) chr5:g.148827328T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827328T>A , CM000667.2:g.148827328T>A GRCh38
NC_000005.9:g.148206891T>A , CM000667.1:g.148206891T>A GRCh37
NC_000005.8:g.148187084T>A NCBI36
NG_016421.1:g.5736T>A
NG_016421.2:g.5736T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.497T>A MANE Select ENSP00000305372.4:p.Phe166Tyr
ENST00000305988.5:c.497T>A ENSP00000305372.4:p.Phe166Tyr
NM_000024.5:c.497T>A NP_000015.1:p.Phe166Tyr
NM_000024.6:c.497T>A MANE Select NP_000015.2:p.Phe166Tyr
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