Canonical Allele Identifier: CA447425465
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1756562218
MyVariant Identifiers: chr5:g.148206745C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827182C>G , CM000667.2:g.148827182C>G GRCh38
NC_000005.9:g.148206745C>G , CM000667.1:g.148206745C>G GRCh37
NC_000005.8:g.148186938C>G NCBI36
NG_016421.1:g.5590C>G
NG_016421.2:g.5590C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.351C>G MANE Select ENSP00000305372.4:p.Val117=
ENST00000305988.5:c.351C>G ENSP00000305372.4:p.Val117=
NM_000024.5:c.351C>G NP_000015.1:p.Val117=
NM_000024.6:c.351C>G MANE Select NP_000015.2:p.Val117=
Search 100 bp 5'
Search 100 bp 3'