Canonical Allele Identifier: CA563960675
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1350387358
gnomAD v2: 5-148206350-C-A
gnomAD v4: 5-148826787-C-A
MyVariant Identifiers: chr5:g.148206350C>A (hg19) chr5:g.148826787C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148826787C>A , CM000667.2:g.148826787C>A GRCh38
NC_000005.9:g.148206350C>A , CM000667.1:g.148206350C>A GRCh37
NC_000005.8:g.148186543C>A NCBI36
NG_016421.1:g.5195C>A
NG_016421.2:g.5195C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000305988.6:c.-45C>A MANE Select ENSP00000305372.4:n.-45C>A
ENST00000305988.5:c.-45C>A ENSP00000305372.4:n.-45C>A
NM_000024.5:c.-45C>A NP_000015.1:n.-45C>A
NM_000024.6:c.-45C>A MANE Select NP_000015.2:n.-45C>A
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