Canonical Allele Identifier: CA447426158
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1756570476
gnomAD v4: 5-148827557-C-G
MyVariant Identifiers: chr5:g.148207120C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827557C>G , CM000667.2:g.148827557C>G GRCh38
NC_000005.9:g.148207120C>G , CM000667.1:g.148207120C>G GRCh37
NC_000005.8:g.148187313C>G NCBI36
NG_016421.1:g.5965C>G
NG_016421.2:g.5965C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.726C>G MANE Select ENSP00000305372.4:p.Val242=
ENST00000305988.5:c.726C>G ENSP00000305372.4:p.Val242=
NM_000024.5:c.726C>G NP_000015.1:p.Val242=
NM_000024.6:c.726C>G MANE Select NP_000015.2:p.Val242=
Search 100 bp 5'
Search 100 bp 3'