Canonical Allele Identifier: CA447425775
Gene: ADRB2 HGNC NCBI

Linked Data

gnomAD v4: 5-148827690-C-T
MyVariant Identifiers: chr5:g.148207253C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827690C>T , CM000667.2:g.148827690C>T GRCh38
NC_000005.9:g.148207253C>T , CM000667.1:g.148207253C>T GRCh37
NC_000005.8:g.148187446C>T NCBI36
NG_016421.1:g.6098C>T
NG_016421.2:g.6098C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.859C>T MANE Select ENSP00000305372.4:p.Leu287=
ENST00000305988.5:c.859C>T ENSP00000305372.4:p.Leu287=
NM_000024.5:c.859C>T NP_000015.1:p.Leu287=
NM_000024.6:c.859C>T MANE Select NP_000015.2:p.Leu287=
Search 100 bp 5'
Search 100 bp 3'