Canonical Allele Identifier: CA447425632
Gene: ADRB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.148207150G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827587G>T , CM000667.2:g.148827587G>T GRCh38
NC_000005.9:g.148207150G>T , CM000667.1:g.148207150G>T GRCh37
NC_000005.8:g.148187343G>T NCBI36
NG_016421.1:g.5995G>T
NG_016421.2:g.5995G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.756G>T MANE Select ENSP00000305372.4:p.Gly252=
ENST00000305988.5:c.756G>T ENSP00000305372.4:p.Gly252=
NM_000024.5:c.756G>T NP_000015.1:p.Gly252=
NM_000024.6:c.756G>T MANE Select NP_000015.2:p.Gly252=