Canonical Allele Identifier: CA361893986
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1252290663
gnomAD v2: 5-148206549-T-C
MyVariant Identifiers: chr5:g.148206549T>C (hg19) chr5:g.148826986T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148826986T>C , CM000667.2:g.148826986T>C GRCh38
NC_000005.9:g.148206549T>C , CM000667.1:g.148206549T>C GRCh37
NC_000005.8:g.148186742T>C NCBI36
NG_016421.1:g.5394T>C
NG_016421.2:g.5394T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305988.6:c.155T>C MANE Select ENSP00000305372.4:p.Val52Ala
ENST00000305988.5:c.155T>C ENSP00000305372.4:p.Val52Ala
NM_000024.5:c.155T>C NP_000015.1:p.Val52Ala
NM_000024.6:c.155T>C MANE Select NP_000015.2:p.Val52Ala
Search 100 bp 5'
Search 100 bp 3'