Canonical Allele Identifier: CA447425686

Gene: ADRB2

Linked Data

• dbSNP Id: rs1277977046
• gnomAD v2: 5-148207190-T-C
• gnomAD v4: 5-148827627-T-C
• MyVariant Identifiers: chr5:g.148207190T>C (hg19) ; chr5:g.148827627T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148827627T>C , CM000667.2:g.148827627T>C	GRCh38
NC_000005.9:g.148207190T>C , CM000667.1:g.148207190T>C	GRCh37
NC_000005.8:g.148187383T>C	NCBI36
NG_016421.1:g.6035T>C
NG_016421.2:g.6035T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305988.6:c.796T>C MANE Select	ENSP00000305372.4:p.Leu266=
ENST00000305988.5:c.796T>C	ENSP00000305372.4:p.Leu266=
NM_000024.5:c.796T>C	NP_000015.1:p.Leu266=
NM_000024.6:c.796T>C MANE Select	NP_000015.2:p.Leu266=