Canonical Allele Identifier: CA361895403
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1756571801
MyVariant Identifiers: chr5:g.148207192G>C (hg19) chr5:g.148827629G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827629G>C , CM000667.2:g.148827629G>C GRCh38
NC_000005.9:g.148207192G>C , CM000667.1:g.148207192G>C GRCh37
NC_000005.8:g.148187385G>C NCBI36
NG_016421.1:g.6037G>C
NG_016421.2:g.6037G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.798G>C MANE Select ENSP00000305372.4:p.Leu266Phe
ENST00000305988.5:c.798G>C ENSP00000305372.4:p.Leu266Phe
NM_000024.5:c.798G>C NP_000015.1:p.Leu266Phe
NM_000024.6:c.798G>C MANE Select NP_000015.2:p.Leu266Phe
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