Canonical Allele Identifier: CA447425444
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1756561746
gnomAD v3: 5-148827143-C-T
gnomAD v4: 5-148827143-C-T
MyVariant Identifiers: chr5:g.148206706C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827143C>T , CM000667.2:g.148827143C>T GRCh38
NC_000005.9:g.148206706C>T , CM000667.1:g.148206706C>T GRCh37
NC_000005.8:g.148186899C>T NCBI36
NG_016421.1:g.5551C>T
NG_016421.2:g.5551C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000305988.6:c.312C>T MANE Select ENSP00000305372.4:p.Phe104=
ENST00000305988.5:c.312C>T ENSP00000305372.4:p.Phe104=
NM_000024.5:c.312C>T NP_000015.1:p.Phe104=
NM_000024.6:c.312C>T MANE Select NP_000015.2:p.Phe104=
Search 100 bp 5'
Search 100 bp 3'