Canonical Allele Identifier: CA447425339
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1481786293
gnomAD v2: 5-148206551-C-T
gnomAD v3: 5-148826988-C-T
gnomAD v4: 5-148826988-C-T
MyVariant Identifiers: chr5:g.148206551C>T (hg19) chr5:g.148826988C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148826988C>T , CM000667.2:g.148826988C>T GRCh38
NC_000005.9:g.148206551C>T , CM000667.1:g.148206551C>T GRCh37
NC_000005.8:g.148186744C>T NCBI36
NG_016421.1:g.5396C>T
NG_016421.2:g.5396C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000305988.6:c.157C>T MANE Select ENSP00000305372.4:p.Leu53=
ENST00000305988.5:c.157C>T ENSP00000305372.4:p.Leu53=
NM_000024.5:c.157C>T NP_000015.1:p.Leu53=
NM_000024.6:c.157C>T MANE Select NP_000015.2:p.Leu53=
Search 100 bp 5'
Search 100 bp 3'