Canonical Allele Identifier: CA129772970
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs201318801
MyVariant Identifiers: chr5:g.148207263T>C (hg19) chr5:g.148827700T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827700T>C , CM000667.2:g.148827700T>C GRCh38
NC_000005.9:g.148207263T>C , CM000667.1:g.148207263T>C GRCh37
NC_000005.8:g.148187456T>C NCBI36
NG_016421.1:g.6108T>C
NG_016421.2:g.6108T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.869T>C MANE Select ENSP00000305372.4:p.Phe290Ser
ENST00000305988.5:c.869T>C ENSP00000305372.4:p.Phe290Ser
NM_000024.5:c.869T>C NP_000015.1:p.Phe290Ser
NM_000024.6:c.869T>C MANE Select NP_000015.2:p.Phe290Ser
Search 100 bp 5'
Search 100 bp 3'