Canonical Allele Identifier: CA805469260
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1381619347
gnomAD v3: 5-148826695-G-C
gnomAD v4: 5-148826695-G-C
MyVariant Identifiers: chr5:g.148206258G>C (hg19) chr5:g.148826695G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148826695G>C , CM000667.2:g.148826695G>C GRCh38
NC_000005.9:g.148206258G>C , CM000667.1:g.148206258G>C GRCh37
NC_000005.8:g.148186451G>C NCBI36
NG_016421.1:g.5103G>C
NG_016421.2:g.5103G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305988.6:c.-137G>C MANE Select ENSP00000305372.4:n.-137G>C
ENST00000305988.5:c.-137G>C ENSP00000305372.4:n.-137G>C
NM_000024.5:c.-137G>C NP_000015.1:n.-137G>C
NM_000024.6:c.-137G>C MANE Select NP_000015.2:n.-137G>C
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