Canonical Allele Identifier: CA129772911
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs866028102
gnomAD v4: 5-148826697-C-G
MyVariant Identifiers: chr5:g.148826697C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148826697C>G , CM000667.2:g.148826697C>G GRCh38
NC_000005.9:g.148206260C>G , CM000667.1:g.148206260C>G GRCh37
NC_000005.8:g.148186453C>G NCBI36
NG_016421.1:g.5105C>G
NG_016421.2:g.5105C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000305988.6:c.-135C>G MANE Select ENSP00000305372.4:n.-135C>G
ENST00000305988.5:c.-135C>G ENSP00000305372.4:n.-135C>G
NM_000024.5:c.-135C>G NP_000015.1:n.-135C>G
NM_000024.6:c.-135C>G MANE Select NP_000015.2:n.-135C>G
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